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calendar

12,921 catalysts · 3,368 8k filing · 2,377 grant · 2,035 approval · 1,373 device 510k · 1,000 device adverse event · 929 device pma

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  • 8k filing3,368
  • grant2,377
  • approval2,035
  • device 510k1,373
  • device adverse event1,000
  • device pma929
device recall
810
  • earnings584
  • recall364
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Nov 24, 2025

    50
    ›Nov 24, 2025device 510k267d agoGuangzhou Potent Medical Equipment Joint-Stock Co., Ltd. — Thulium Fiber Laser System (TFL-A); Thulium Fiber Laser System (TFL-B) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 24, 2025device 510k267d agoGuangzhou Potent Medical Equipment Joint-Stock Co., Ltd. — Holmium Laser System (Potent HP90); Holmium Laser System (Potent HP100); Holmium Laser System (Potent HP9120); Holmium Laser System (Potent HP140); Holmium Laser System (Potent HP150) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 24, 2025device 510k267d agoLaerdal Medical AS — The BAG manual resuscitator and accessories (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 24, 2025device 510k267d agoAngioDynamics, Inc. — AlphaVac Multipurpose Mechanical Aspiration System F1885 (510k cleared)ANGIODYNAMICS INC

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

    full page →fda device 510k ↗
    ›Nov 24, 2025device 510k267d agoEurosets S.R.L — Trilly Pediatric Oxygenator with Integrated Arterial Filter (US5232) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 24, 2025device 510k267d agoF Care Systems USA, LLC — F Care RF System (00MEDRF4000US, 05RAFAELOPROBE, 05SPHERAPROBE, 06OUTPUTKAB, 06Pedal1St) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 24, 2025device 510k267d agoGE Medical Systems Ultrasound and Primary Care Diagnostics — Voluson Expert 18; Voluson Expert 20; Voluson Expert 22 (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 24, 2025device 510k267d agoA2z Radiology Ai, Inc. — a2z-Unified-Triage (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 24, 2025device 510k267d agoVesalio, Inc. — NeVa PV Thrombectomy Device (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 24, 2025device 510k267d agoBozhou Rongjian Medical Appliance Co., Ltd. — Transcutaneous Electrical Nerve Stimulator (RJTENS-2) (510k cleared)

    Product code: NUH. Advisory committee: Neurology. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 24, 2025device 510k267d agoFresenius Medical Care Renal Therapies Group, LLC — BCM2-Body Composition Monitor (510k cleared)Fresenius Medical Care AG

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

    full page →fda device 510k ↗
    ›Nov 24, 2025device pma267d agoW. L. Gore & Associates, Inc. — GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 24, 2025device pma267d agoHologic, Inc. — Envision Mammography Platform (PMA supplement)

    Supplement type: Normal 180 Day Track No User Fee. Product code: OTE. Advisory committee: RA. Decision: APPR

    full page →fda device pma ↗
    ›Nov 24, 2025device pma267d agoThe Spectranetics Corp. — Stellarex 0.035 OTW Drug-Coated Angioplasty Balloon (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 24, 2025device pma267d agoExact Sciences Corporation — Cologuard® (PMA supplement)

    Supplement type: Real-Time Process. Product code: PHP. Advisory committee: PA. Decision: APPR

    full page →fda device pma ↗
    ›Nov 24, 2025device pma267d agoOcclutech Holding AG — Occlutech ASD Occluder; Occlutech Pistol Pusher (OPP); Occlutech ASD Occluder Procedure Pack (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 24, 2025device recall267d agoSmith & Nephew, Inc. device recall (Cls II)SMITH & NEPHEW PLC

    BIOSURE HA SCREW, 6MM x 20 MM. Threaded metallic bone fixation fastener. — Reason: Removal of affected lot of screws due to labeling error. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoICU Medical, Inc. device recall (Cls II)ICU MEDICAL INC/DE

    LifeShield Drug Library Management (DLM); LifeShield Infusion Safety Software Suite v2.2 List Number 17003-02 — Reason: For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been completed. Users must use alternate methods to review changes. Failure to do so may lead in over delivery, under delivery, or delay in setup on the infusion pump. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoZimmer Surgical Inc device recall (Cls II)

    Zimmer Air Dermatome, Model/Catalog Number: 00880100100 — Reason: The devices may have a misaligned thickness control bar. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoDraeger, Inc. device recall (Cls I)Traeger, Inc.

    Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer. — Reason: A certain component of affected devices was not delivered within specification and contained impurities. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoICU Medical, Inc. device recall (Cls II)ICU MEDICAL INC/DE

    LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software Suite v2.2 Product No. 17003-02 — Reason: Software issue only allows Concentration Limits to be defined to one digit of precision past the decimal point (0.1) instead of three digits (0.001). If the user is unable to use Concentration Limits as intended, they may need to change the limits to something other than what is recommended by the drug manufacturer, which may result in over- or under-delivery. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoAbbott Diabetes Care, Inc. device recall (Cls I)TANDEM DIABETES CARE INC

    FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System. — Reason: Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoZimmer Surgical Inc device recall (Cls II)

    Zimmer Dermatome AN, Model/Catalog Number: 88710100 — Reason: The devices may have a misaligned thickness control bar. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoAbbott Diabetes Care, Inc. device recall (Cls I)TANDEM DIABETES CARE INC

    FreeStyle Libre 3 Plus Sensor REF 78768-01 UDI-DI code: 00357599844011 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System. — Reason: Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoAlcon Research LLC device recall (Cls I)Alcon Laboratories Inc

    Brand Name: Alcon Laboratories, Inc. Product Name: Custom Pak Model/Catalog Numbers: 9903-20, 17188-04, 19762-03, 19203-04, 19203-04, 17957-10 Software Version: N/A Product Description: Alcon Custom Paks are customer-designed sterile surgical procedure packs / convenience kits intended for use by trained ophthalmic surgeons in a variety of ophthalmic surgeries. Custom Pak is a collection of various ophthalmic surgical instruments and the necessary materials necessary to perform an ophthalmic surgical procedure. Component: N/A — Reason: Ophthalmic procedure packs may have incomplete seals affecting sterility. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoDraeger, Inc. device recall (Cls I)Traeger, Inc.

    Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer. — Reason: A certain component of affected devices was not delivered within specification and contained impurities. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoAbbott Diabetes Care, Inc. device recall (Cls I)TANDEM DIABETES CARE INC

    FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System. — Reason: Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoAbbott Diabetes Care, Inc. device recall (Cls I)TANDEM DIABETES CARE INC

    FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System. — Reason: Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 25, 2025approval266d agoHYDROCODONE BITARTRATE AND ACETAMINOPHEN (ACETAMINOPHEN) — FDA approvalIGC Pharma, Inc.

    Sponsor: AMNEAL PHARMS NY. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoTIZANIDINE HYDROCHLORIDE — FDA approvalZydus Therapeutics Inc

    Sponsor: ZYDUS PHARMS. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoHUMATROPE (SOMATROPIN) — FDA approvalEMD Serono Inc

    Sponsor: LILLY. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoPRED MILD (PREDNISOLONE ACETATE) — FDA approvalprednisolone acetate

    Sponsor: ABBVIE. Form: SUSPENSION/DROPS. Route: OPHTHALMIC

    full page →prednisolone acetate →fda approvals ↗
    ›Nov 25, 2025approval266d agoZEGERID OTC (OMEPRAZOLE) — FDA approvalCovis Pharmaceuticals Inc (Inactive)

    Sponsor: RILEY CONSUMER. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoENOXAPARIN SODIUM (PRESERVATIVE FREE) (ENOXAPARIN SODIUM) — FDA approvalenoxaparin sodium

    Sponsor: SHENZHEN TECHDOW. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →enoxaparin sodium →fda approvals ↗
    ›Nov 25, 2025approval266d agoIRBESARTAN — FDA approvalIRBESARTAN

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

    full page →IRBESARTAN →fda approvals ↗
    ›Nov 25, 2025approval266d agoSCEMBLIX (ASCIMINIB HYDROCHLORIDE) — FDA approvalasciminib hydrochloride

    Sponsor: NOVARTIS. Form: TABLET. Route: ORAL

    full page →asciminib hydrochloride →fda approvals ↗
    ›Nov 25, 2025approval266d agoVOYXACT (SIBEPRENLIMAB-SZSI) — FDA approvalsibeprenlimab

    Sponsor: OTSUKA PHARM CO LTD. Form: INJECTABLE. Route: INJECTION

    full page →sibeprenlimab →fda approvals ↗
    ›Nov 25, 2025approval266d agoIMFINZI (DURVALUMAB) — FDA approvalASTRAZENECA PLC

    Sponsor: ASTRAZENECA UK LTD. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoACETAZOLAMIDE — FDA approvalAccord Healthcare Inc

    Sponsor: HIBROW HLTHCARE. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoCHILDREN'S CETIRIZINE HYDROCHLORIDE HIVES RELIEF (CETIRIZINE HYDROCHLORIDE) — FDA approvalKenvue Inc.

    Sponsor: BAJAJ. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoPERAMPANEL — FDA approvalCATALYST PHARMACEUTICALS, INC.

    Sponsor: TARO. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoNOREPINEPHRINE BITARTRATE — FDA approvalBaxter Healthcare Corp

    Sponsor: ANTHEA PHARMA. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoIRBESARTAN AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) — FDA approvalALDACTAZIDE

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

    full page →ALDACTAZIDE →fda approvals ↗
    ›Nov 25, 2025approval266d agoPERAMPANEL — FDA approvalPERAMPANEL

    Sponsor: MSN. Form: TABLET. Route: ORAL

    full page →PERAMPANEL →fda approvals ↗
    ›Nov 25, 2025device 510k266d agoOlympus Medical Systems Corporation — Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M) (510k cleared)

    Product code: KNS. Advisory committee: Gastroenterology, Urology. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoIndica Labs, LLC — HALO AP Dx (510k cleared)

    Product code: QKQ. Advisory committee: Pathology. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoEncore Guards — enCore Night Guard (510k cleared)

    Product code: OBR. Advisory committee: Unknown. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoStemtech Medical Devices Private Limited — Eva Scalp Cooling System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoAkura Medical — Akura Thrombectomy System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoGood Sleep CO Pte , Ltd. — Hushd Avera (510k cleared)

    Product code: LRK. Advisory committee: Dental. Type: Abbreviated

    full page →fda device 510k ↗
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    $SNN29.76-0.17%
    $FMS23.59-0.78%
    $ANGO13.82-2.81%
    $COOK
    $ICUI183.67+0.38%
    $TNDM22.86+0.62%
    $TNDM22.86+0.62%
    $ICUI183.67+0.38%
    $TNDM22.86+0.62%
    $TNDM22.86+0.62%
    $COOK
    $IGC0.2670+0.41%
    $ABBV249.42-0.06%
    $NVS150.88-0.55%
    $AZN156.58+0.08%
    $KVUE18.79-2.14%
    $CPRX31.490.00%