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18,279 catalysts · 4,728 grant · 3,111 8k filing · 2,643 approval · 2,206 device 510k · 1,789 device recall · 1,544 device pma

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  • grant4,728
  • 8k filing3,111
  • approval2,643
  • device 510k2,206
  • device recall1,789
  • device pma1,544
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1,000
  • recall593
  • earnings583
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    • Oncology148
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    • Pulmonology22
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    Week of Aug 4, 2025

    50
    ›Aug 4, 2025device 510k373d agoSpectrum Medical S.R.L. — Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG) (510k cleared)

    Product code: KFM. Advisory committee: Cardiovascular. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 4, 2025device 510k373d agoAndon Health Co, Ltd. — iHealth Compare Wireless Blood Pressure Monitor(BP-300C);iHealth Compare Pro Wireless Blood Pressure Monitor(BP-300CV);iHealth Compare S Wireless Blood Pressure Monitor(BP-300V);iHealth Wireless Blood Pressure Monitor(BPX1);iHealth Blood Pressure Monitor(KD-595);iHealth Track Pro Connected Blood Pressure Monitor(KN-550LT);Semi Automatic Blood Pressure Monitor(KD-388N);Arm Blood Pressure Monitor(KD-553);Arm Blood Pressure Monitor(KD-557BR);Arm Blood Pressure Monitor(KD-558);Arm Blood Pr (510k cleared)

    Product code: DXN. Advisory committee: Cardiovascular. Type: Abbreviated

    full page →fda device 510k ↗
    ›Aug 4, 2025device 510k373d agoOkapi Medical, LLC Dba Resivant Medical — CUTIVA™ Topical Skin Adhesive (RM1700); CUTIVA™ PLUS Skin Closure System (RM1739) (510k cleared)

    Product code: MPN. Advisory committee: General, Plastic Surgery. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 4, 2025device 510k373d agoDaxor Corporation — Blood Volume Analyzer (200) (510k cleared)DAXOR CORP

    Product code: JWO. Advisory committee: Hematology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 4, 2025device 510k373d agoH&abyz Co., Ltd. — HnX-P1, HnX-PB (510k cleared)

    Product code: IZL. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 5, 2025approval372d agoDAYBUE (TROFINETIDE) — FDA approvaltrofinetide

    Sponsor: ACADIA PHARMS INC. Form: SOLUTION. Route: ORAL

    full page →trofinetide →fda approvals ↗
    ›Aug 5, 2025approval372d agoDAYBUE (TROFINETIDE) — FDA approvaltrofinetide

    Sponsor: ACADIA PHARMS INC. Form: SOLUTION. Route: ORAL

    full page →trofinetide →fda approvals ↗
    ›Aug 5, 2025approval372d agoPOMALIDOMIDE — FDA approvalTeva Pharmaceuticals USA Inc

    Sponsor: TEVA PHARMS USA. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Aug 5, 2025approval372d agoPOMALIDOMIDE — FDA approvalPOMALIDOMIDE

    Sponsor: MYLAN. Form: CAPSULE. Route: ORAL

    full page →POMALIDOMIDE →fda approvals ↗
    ›Aug 5, 2025device pma372d agoInstylla, Inc. — Embrace(TM) Hydrogel Embolic System (PMA)

    Product code: QVG. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 5, 2025device pma372d agoDePuy Orthopaedics, Inc. — CERAMAX CERAMIC HIP SYSTEM (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MRA. Advisory committee: OR. Decision: OK30

    full page →fda device pma ↗
    ›Aug 5, 2025device pma372d agoTerumo Medical Corporation — MISAGO® RX Self-expanding Peripheral Stent; R2P Misago RX Self-expanding Peripheral Stent System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: NIP. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Aug 5, 2025device pma372d agoMedtronic Vascular, Inc. — EVERFLEX SELF-EXPANDING PERIPHERAL STENT SYSTEM (EVERFLEX) (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: NIP. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 5, 2025device pma372d agoDepuy, Inc. — LCS® Total Knee System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: NJL. Advisory committee: OR. Decision: OK30

    full page →fda device pma ↗
    ›Aug 5, 2025device pma372d agoSirtex Medical, Inc. — Lava Liquid Embolic System (Lava LES) and Lava Mixing Kit (PMA supplement)

    Supplement type: Real-Time Process. Product code: QVG. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 5, 2025device pma372d agoAbbott Molecular, Inc. — Vysis ALK Break Apart FISH Probe Kit (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: OWE. Advisory committee: PA. Decision: APPR

    full page →fda device pma ↗
    ›Aug 5, 2025device pma372d agoSmith & Nephew, Inc. — ASCENSION MCP (PMA supplement)SMITH & NEPHEW PLC

    Supplement type: 30-Day Notice. Product code: NEG. Advisory committee: OR. Decision: OK30

    full page →fda device pma ↗
    ›Aug 5, 2025device pma372d agoTeleflex Medical, LLC — MANTA™ Vascular Closure Device; MANTA Vascular Closure Device, 18F; MANTA Vascular Closure Device, 14F; MANTA SF Depth L (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MGB. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Aug 5, 2025device recall372d agoBoston Scientific Corporation device recall (Cls II)BOSTON SCIENTIFIC CORP

    Boston Scientific NephroMax Kit, Material Numbers (UPN): 1. M0062101180; 2. M0062101600. (Urology) — Reason: The Encore 26 Inflation Device is used with balloon dilation catheters to create and monitor pressure in the balloon and to deflate the balloon. An internal investigation determined that during use, foreign material particles could migrate from affected Encore 26 Inflation Devices into a balloon dilatation catheter. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoIntegra LifeSciences Corp. (NeuroSciences) device recall (Cls II)INTEGRA LIFESCIENCES HOLDINGS CORP

    Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿ Paste with Active Leptospermum Honey is a moist dressing made of 100% Active Leptospermum medical grade Honey. The dressing helps maintain a moist environment conducive to wound healing and helps aid and support autolytic debridement. The dressing can be removed without causing trauma to the wound when a primary dressing is used. — Reason: Packaging failures were identified which could lead to a breach in the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoAlcon Research LLC device recall (Cls II)Alcon Laboratories Inc

    Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065750918 PAK,I/A LINE,NGVS 8065750957 ASSY,SHIP,CONSTELLATION VFC 8065750972 ENDOILLUMATOR,RFID,23G 8065751014 CONST AUTO GAS FILL PAK 8065751014 CONST AUTO GAS FILL PAK 8065751441 ENDOILLUMINATOR,RFID,25G 8065751577 CHANDELIER,25GA,W/RFID Software Version: N/A Product Description: These products are standalone accessory devices meant for vitrectomy surgical procedures. They interface with a corresponding Alcon surgical console. Component: N/A — Reason: Due to incomplete seals in the pouch which provide the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoTandem Diabetes Care, Inc. device recall (Cls II)TANDEM DIABETES CARE INC

    t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014070, 1014071, 1014072, 1014073, and User Guide when using Dexcom G7 sensor; Tandem Mobi insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014801, 1014811, 1014813, and User Guide when using Dexcom G7 sensor — Reason: A software defect in versions 7.9.0.1 and 7.10.1 of the pump software for Tandem t:slim X2 and version 7.9.0.1 of the Tandem Mobi pump with Control-IQ+ technology that are paired with a G7 sensor may result in an unexpected automatic insulin correction bolus (autobolus ) which could result in hypoglycemia. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoPhilips Medical Systems (Cleveland) Inc device recall (Cls II)

    Pinnacle Radiation Therapy Planning System: Multimodality Simulation Workspace 18.0.5 Model 870258 UDI code: (01)00884838103566(10)18.0.5.22236 Pinnacle TumorLOC 16.2 Model 870226 UDI code: (01)00884838091122(10)16.2.0.60010 Pinnacle TumorLOC 16.2.1 Model 870227 UDI code: (01)00884838091122(10)16.2.1.60098 Pinnacle TumorLOC 16.0.2 Model 870218 UDI code: (01)00884838085602(10)16.0.2.60004 Pinnacle TumorLOC 14.0 Model 870200 UDI code: N/A Pinnacle3 Radiation Therapy Planning System is a software package intended to provide planning support for the treatment of disease processes. The full Pinnacle3 Radiation Therapy Planning System software package provides planning support for the treatment of disease processes, utilizing photon, electron and brachytherapy techniques. — Reason: Due to a software issue, there is a potential image error of the Region of Interest for expansion/contraction for HFP (Head First Prone), FFS (Feet First Supine) and FFP (Feet First Prone) orientations. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoIntegra LifeSciences Corp. (NeuroSciences) device recall (Cls II)INTEGRA LIFESCIENCES HOLDINGS CORP

    Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Model/Catalog Number: 9370613, 937404 Product Description: Infused with natural medical-grade honey Manuka (Leptospermum) honey is a medical-grade honey that is harvested from bees in New Zealand. Researchers have found that this species has unique components that make it ideal for wounds. — Reason: Packaging failures were identified which could lead to a breach in the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoAlcon Research LLC device recall (Cls II)Alcon Laboratories Inc

    Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065000252 UNITY 27 GA CHANDELIER 8065000253 UNITY 27+DS WIDE ANGLE LIGHT PROBE Software Version: N/A Product Description: These products are standalone accessory devices meant for vitrectomy surgical procedures. They interface with a corresponding Alcon surgical console. Component: N/A — Reason: Due to incomplete seals in the pouch which provide the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoIntegra LifeSciences Corp. (NeuroSciences) device recall (Cls II)INTEGRA LIFESCIENCES HOLDINGS CORP

    Brand Name: MediHoney¿ Product Name: MediHoney¿ Adhesive Hydrogel Sheet Dressing Model/Catalog Number: 31720, 31740 Product Description: MEDIHONEY¿ Adhesive Hydrogel Sheet Dressing with Leptospermum Honey is a moist wound dressing made of Leptospermum Honey (+15) in combination with a hydrogel gelling agent, surrounded by an adhesive border. The gelling agent is contained within the dressing mass. The dressing contains 100% Leptospermum Honey. As wound exudate is absorbed, the dressing which has a low pH and high osmolarity forms a gel. This assists in maintaining a moist environment for optimal wound healing, aids in autolytic debridement, and allows for non-traumatic removal. This product is an occlusive dressing, and does not require a secondary dressing. — Reason: Packaging failures were identified which could lead to a breach in the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoAlcon Research LLC device recall (Cls II)Alcon Laboratories Inc

    Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065000393 UNITY HP VISCOUS FLUID CONTROL VFC PACK Software Version: N/A Product Description: These products are standalone accessory devices meant for vitrectomy surgical procedures. They interface with a corresponding Alcon surgical console. Component: N/A — Reason: Due to incomplete seals in the pouch which provide the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoBoston Scientific Corporation device recall (Cls II)BOSTON SCIENTIFIC CORP

    Boston Scientific UroMax Ultra Kit, Material Numbers (UPN): 1. M0062251200, 2. M0062251210, 3. M0062251220, 4. M0062251230, 5. M0062251240, 6. M0062251260, 7. M0062251290, 8. M0062251300, 9. M0062251310. 10. M0062251350, 11. M0062251360, 12. M0062251370. (Urology) — Reason: The Encore 26 Inflation Device is used with balloon dilation catheters to create and monitor pressure in the balloon and to deflate the balloon. An internal investigation determined that during use, foreign material particles could migrate from affected Encore 26 Inflation Devices into a balloon dilatation catheter. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoBoston Scientific Corporation device recall (Cls II)BOSTON SCIENTIFIC CORP

    Boston Scientific Encore 26 Inflation Device, Material Numbers (UPN): 1. H74904526011; 2. H74904526052; 3. M0067101140; 4. M001151050; 5. M001151062; 6. M00566670. (Interventional Cardiology, Peripheral Interventions) — Reason: The Encore 26 Inflation Device is used with balloon dilation catheters to create and monitor pressure in the balloon and to deflate the balloon. An internal investigation determined that during use, foreign material particles could migrate from affected Encore 26 Inflation Devices into a balloon dilatation catheter. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoIntegra LifeSciences Corp. (NeuroSciences) device recall (Cls II)INTEGRA LIFESCIENCES HOLDINGS CORP

    Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Sheet Dressing with Leptospermum Model/Catalog Number: 31612, 31622, 31644 Product Description: MEDIHONEY¿ HCS SHEET DRESSING with LEPTOSPERMUM HONEY is a moist wound dressing made of Leptospermum Honey (+15) in combination with a hydrogel collodial gelling agent. The gelling agent is contained within the dressing mass. The dressing contains 63%, by weight, Leptospermum Honey. As wound exudate is absorbed, the dressing which has a low pH and high osmolarity forms a gel. This assists in maintaining a moist environment for optimal wound healing, aids in autolytic debridement, and allows for non-traumatic removal. This product is an occlusive dressing, and does require a secondary dressing. — Reason: Packaging failures were identified which could lead to a breach in the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoIntegra LifeSciences Corp. (NeuroSciences) device recall (Cls II)INTEGRA LIFESCIENCES HOLDINGS CORP

    Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Model/Catalog Number: 31620, 31640 Product Description: MEDIHONEY¿ Non-Adhesive Hydrogel Sheet Dressing with Leptospermum Honey is a moist wound dressing made of Leptospermum Honey (+15) in combination with a hydrogel gelling agent. The gelling agent is contained within the dressing mass. The dressing contains 100%, Leptospermum Honey. As wound exudate is absorbed, the dressing which has a low pH and high osmolarity forms a gel. This assists in maintaining a moist environment for optimal wound healing, aids in autolytic debridement, and allows for non-traumatic removal. This product is an occlusive dressing, and does require a secondary dressing. — Reason: Packaging failures were identified which could lead to a breach in the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoAlcon Research LLC device recall (Cls II)Alcon Laboratories Inc

    Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065000250 UNITY 27+DS HYPERVIT 30K VIT PROBE 8065753168 UNITY 25+ 7.5K ANTERIOR VIT PROBE 8065753179 UNITY 25+ HYPERVIT 30K VIT PROBE Software Version: N/A Product Description: These products are standalone accessory devices meant for vitrectomy surgical procedures. They interface with a corresponding Alcon surgical console. Component: N/A — Reason: Due to incomplete seals in the pouch which provide the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoIntegra LifeSciences Corp. (NeuroSciences) device recall (Cls II)INTEGRA LIFESCIENCES HOLDINGS CORP

    Brand Name: MediHoney ¿ Product Name: MediHoney ¿ Tube Model/Catalog Number: 31515 and 31535 Product Description: MediHoney¿ Paste with Active Leptospermum Honey is a moist dressing made of 100% Active Leptospermum medical grade Honey. The dressing helps maintain a moist environment conducive to wound healing and helps aid and support autolytic debridement. The dressing can be removed without causing trauma to the wound when a primary dressing is used. — Reason: Packaging failures were identified which could lead to a breach in the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoIntegra LifeSciences Corp. (NeuroSciences) device recall (Cls II)INTEGRA LIFESCIENCES HOLDINGS CORP

    Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Surgical Adhesive Sheet Model/Catalog Number: 31738 Product Description: MEDIHONEY¿ HCS SURGICAL ADHESIVE SHEET DRESSINGS with LEPTOSPERMUM HONEY is a moist wound dressing made of Leptospermum Honey (+15) in combination with a hydrogel colloidal gelling agent, surrounded by an adhesive border. The gelling agent is contained within the dressing mass. As wound exudate is absorbed, the dressing which has a low pH and high osmolarity forms a gel. This assists in maintaining a moist environment for optimal wound healing, aids and supports autolytic debridement, and allows for non-traumatic removal. The product is an occlusive dressing, and does not require a secondary dressing. — Reason: Packaging failures were identified which could lead to a breach in the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoIntegra LifeSciences Corp. (NeuroSciences) device recall (Cls II)INTEGRA LIFESCIENCES HOLDINGS CORP

    Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Adhesive Sheet Model/Catalog Number: 31722, 31744 Product Description: MEDIHONEY¿ HCS ADHESIVE SHEET DRESSING with LEPTOSPERMUM HONEY is a moist wound dressing made of Leptospermum Honey (+15) in combination with a hydrogel colloidal gelling agent, surrounded by an adhesive border. The gelling agent is contained within the dressing mass. The dressing contains 63%, by weight, Leptospermum Honey. As wound exudate is absorbed, the dressing which has a low pH and high osmolarity forms a gel. This assists in maintaining a moist environment for optimal wound healing, aids in autolytic debridement, and allows for non-traumatic removal. This product is an occlusive dressing, and does not require a secondary dressing. — Reason: Packaging failures were identified which could lead to a breach in the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoBoston Scientific Corporation device recall (Cls II)BOSTON SCIENTIFIC CORP

    Boston Scientific Encore Advantage Kit, Material Numbers (UPN): 1. H74904527011; 2. H74904527052. (Interventional Cardiology and Peripheral Interventions) — Reason: The Encore 26 Inflation Device is used with balloon dilation catheters to create and monitor pressure in the balloon and to deflate the balloon. An internal investigation determined that during use, foreign material particles could migrate from affected Encore 26 Inflation Devices into a balloon dilatation catheter. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device recall372d agoAlcon Research LLC device recall (Cls II)Alcon Laboratories Inc

    Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065000356 27GA HP ENTRY SYSTEM, 4 MM 1 COUNT 8065000358 25GA HP ENTRY SYSTEM, 6 MM 1 COUNT 8065000359 27GA HP ENTRY SYSTEM, 6 MM 1 COUNT 8065000467 25GA INFUSION CANNULA(4&6MM ES)+TRAY+TMD 8065000468 27GA INFUSION CANNULA(4&6MM ES)+TRAY+TMD Software Version: N/A Product Description: These products are standalone accessory devices meant for vitrectomy surgical procedures. They interface with a corresponding Alcon surgical console. Component: N/A — Reason: Due to incomplete seals in the pouch which provide the sterile barrier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 5, 2025device 510k372d agoNanosonics — trophon2 (510k cleared)

    Product code: OUJ. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 5, 2025device 510k372d agoShanghai United Imaging Healthcare Co., Ltd. — uMR Jupiter (510k cleared)

    Product code: LNH. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 5, 2025device 510k372d agoEncore Medical L.P. — AltiVate Reverse® Glenoid (510k cleared)Encore Medical, Inc.

    Product code: PHX. Advisory committee: Orthopedic. Type: Special

    full page →fda device 510k ↗
    ›Aug 5, 2025device 510k372d agoClaritas Healthtech Pte, Ltd. — iPETcertum (v1.0) (510k cleared)

    Product code: LLZ. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 5, 2025device 510k372d agoSimplivia Healthcare , Ltd. — Chemfort Female Luer Lock Adaptor (510k cleared)

    Product code: ONB. Advisory committee: General Hospital. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 5, 2025device 510k372d agoBethesda Medical Devices — PRADO™ Lumbar Interbody Fusion System (510k cleared)

    Product code: MAX. Advisory committee: Orthopedic. Type: Special

    full page →fda device 510k ↗
    ›Aug 5, 2025device 510k372d agoRespiree Pte, Ltd. — Respiree Cardio- Respiratory Monitor System (510k cleared)

    Product code: BZQ. Advisory committee: Anesthesiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 6, 2025approval371d agoCOSENTYX (SECUKINUMAB) — FDA approvalNOVARTIS AG

    Sponsor: NOVARTIS PHARMS CORP. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Aug 6, 2025approval371d agoCOSENTYX (SECUKINUMAB) — FDA approvalNOVARTIS AG

    Sponsor: NOVARTIS PHARMS CORP. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Aug 6, 2025approval371d agoLAMOTRIGINE — FDA approvalLAMOTRIGINE

    Sponsor: GLENMARK PHARMS LTD. Form: TABLET. Route: ORAL

    full page →LAMOTRIGINE →fda approvals ↗
    ›Aug 6, 2025approval371d agoLAMOTRIGINE — FDA approvalTorrent Pharma Inc

    Sponsor: UNICHEM LABS LTD. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Aug 6, 2025approval371d agoIBANDRONATE SODIUM — FDA approvalDR REDDYS LABORATORIES LTD

    Sponsor: PHARMOBEDIENT. Form: INJECTABLE. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Aug 6, 2025approval371d agoZTALMY (GANAXOLONE) — FDA approvalganaxolone

    Sponsor: IMMEDICA PHARMA. Form: SUSPENSION. Route: ORAL

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    $ACAD29.38-0.03%
    $DXR
    $TNDM23.07+1.14%
    $IART17.43+2.11%
    $SNN30.11+0.12%
    $BSX51.32+1.70%
    $ACAD29.38-0.03%
    $BSX51.32+1.70%
    $BSX51.32+1.70%
    $IART17.43+2.11%
    $IART17.43+2.11%
    $IART17.43+2.11%
    $IART17.43+2.11%
    $IART17.43+2.11%
    $IART17.43+2.11%
    $IART17.43+2.11%
    $EMI
    $BSX51.32+1.70%
    $RDY12.45+2.43%
    $NVS155.21-1.01%
    $NVS155.21-1.01%