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calendar

18,238 catalysts · 4,728 grant · 3,230 8k filing · 2,627 approval · 2,156 device 510k · 1,745 device recall · 1,501 device pma

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  • grant4,728
  • 8k filing3,230
  • approval2,627
  • device 510k2,156
  • device recall1,745
  • device pma1,501
device adverse event
1,000
  • recall586
  • earnings584
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  • therapy area
    • Oncology148
    • Infectious Disease46
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    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Aug 25, 2025

    38
    ›Aug 29, 2025device pma350d agoABBOTT MEDICAL — Proclaim™ Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LGW. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Aug 29, 2025device pma350d agoMedtronic, Inc. — SynchroMed Infusion System, Ascenda Intrathecal Catheters (PMA supplement)Medtronic plc

    Supplement type: Special (Immediate Track). Product code: LKK. Advisory committee: HO. Decision: APPR

    full page →fda device pma ↗
    ›Aug 29, 2025device pma350d agoMedtronic Minimed, Inc. — MiniMed 780G System (PMA supplement)Medtronic USA Inc

    Supplement type: Panel Track. Product code: OZP. Advisory committee: CH. Decision: APPR

    full page →fda device pma ↗
    ›Aug 29, 2025device pma350d 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 29, 2025device pma350d agoW. L. Gore & Associates, Inc. — GORE® TAG® Conformable Thoracic Stent Graft with ACTIVE CONTROL System (CMDS) 00733132646890; 00733132646906; 007331326 (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 29, 2025device pma350d agoMedtronic, Inc. — Sphere-9 Catheter Mapping and Ablation Catheter (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Aug 29, 2025device pma350d agoW. L. Gore and Associates, Inc. — GORE® EXCLUDER® Conformable AAA Endoprosthesis (EXCC) 00733132650927; 00733132650934; 00733132650941; 00733132650958; 00 (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 29, 2025device pma350d agoABBOTT MEDICAL — Proclaim™ Doral Root Ganglion (DRG) IPG (PMA supplement)GALT Pharmaceuticals LLC

    Supplement type: 30-Day Notice. Product code: PMP. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Aug 29, 2025device pma350d agoABBOTT MEDICAL — Esprit™ BTK Everolimus Eluting Resorbable Scaffold System (PMA supplement)Postsurgical Therapeutics Inc

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

    full page →fda device pma ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK System Solution Set, DUO-VENT, CLEARLINK Luer Activated Valve, 10 drops/mL, 92-inch (2.3 meters), Product code 2C8419 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoNortheast Scientific Inc. device recall (Cls II)

    NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-156. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US. — Reason: Potential for breaches in the sterile barrier packaging, compromising sterility assurance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoNortheast Scientific Inc. device recall (Cls II)

    NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-006. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US. — Reason: Potential for breaches in the sterile barrier packaging, compromising sterility assurance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, Retractable Collar, 10 drops/mL, 120-inch (3.0 meters), Product Code 2C8541 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBigTree Sales Inc. device recall (Cls II)

    The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range. — Reason: The subject product emits unsafe level of UVC radiation (i.e., the product reaches the exposure limit for Risk Group 3 (high risk) in about 2.2 minutes). The product has a radiation safety defect, in that these radiation emissions are unnecessary to the accomplishment of the product s primary purpose of disinfecting objects and surfaces, and create a risk of skin and/or eye injuries to user and nearby persons. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, two CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 104-inch (2.6 meters), Product Code 2C8571 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoNortheast Scientific Inc. device recall (Cls II)

    NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-420-159. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US. — Reason: Potential for breaches in the sterile barrier packaging, compromising sterility assurance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoGetinge Disinfection Ab device recall (Cls II)

    Getinge 88-Series Washer- Disinfector. Model Number: 88-5. — Reason: Potential for device to overheat during operation if the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure alarm is not triggered. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable Collar, 14-inch (35 centimeters), Product Code 2C8632 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, Retractable Collar, 10 drops/mL, 120-inch (3.0 meters), Product Code 2C8537 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 120-inch (3.0 meters), Non-DEHP, Product Code 2R8537 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM NON-DEHP CONTINU-FLO SOLN SET, 96" (2,4 m), Product Code: 2H8519 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoImaCor Inc. device recall (Cls II)

    ClariTEE Miniaturized TEE probe. Model Number: CLT-010. Ultrasound miniaturized TEE probe for use with Mobile Ultrasound, ImaCor model ZHH. — Reason: Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex, and vice versa. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoNortheast Scientific Inc. device recall (Cls II)

    NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-410-152. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. — Reason: Potential for breaches in the sterile barrier packaging, compromising sterility assurance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK System Paclitaxel Set, Non-Vented with Polyethylene Lined Tubing and CLEARLINK Luer Activated Valve, 0.2 Micron Filter, CLEARLINK Luer Activated Valve, 10 drops/mL, 107-inch (2.7 meters), Product Code 2R8858 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, Plus 4-Way Stopcock Extension Set with two CLEARLINK Luer Activated Valve, Pfoduct code 2C6255 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable Collar, 44-inch (111 centimeters), Product code 2C8610 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK System Non_DEHP Extenstion Set, Straight-Type Extension Set, Standard Bore, 1.2 Micron Filter, CLEARLINK Luer Activated Valve, 19-inch (47 centimeters), Product Code 2H8603 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoNortheast Scientific Inc. device recall (Cls II)

    NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-151. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US. — Reason: Potential for breaches in the sterile barrier packaging, compromising sterility assurance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoNortheast Scientific Inc. device recall (Cls II)

    NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-414-159. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US. — Reason: Potential for breaches in the sterile barrier packaging, compromising sterility assurance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoNortheast Scientific Inc. device recall (Cls II)

    NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter. Model/Catalog Number: R-410-154. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US. — Reason: Potential for breaches in the sterile barrier packaging, compromising sterility assurance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 112-inch (2.8 meters), Product Code 2C8519 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, three CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 102-inch (2.6 meters), Product Code 2C8593 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoFresenius Medical Care Holdings, Inc. device recall (Cls II)Fresenius Medical Care AG

    Optiflux¿ High Flux E-beam Dialyzer Model Numbers: (1) 0500316E OPTIFLUX F160NRe 12/CS 1.5SA EBEAM, (2) 0500318E OPTIFLUX F180NRe 12/CS 1.7SA EBEAM, (3) 0500320E OPTIFLUX F200NRe 12/CS 1.9SA EBEAM, (4) 0500325E OPTIFLUX F250NRe 12/CS 2.5SA EBEAM — Reason: To provide further information to the user to ensure proper use of the medical device. the caps had been changed from a threaded version to a press-on version whereby the user must press the caps firmly onto the dialyzer to securely affix the cap. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoConvaTec, Inc device recall (Cls II)

    DuoDERM" Extra Thin dressings are highly flexible, control gel formula dressings designed for use on dry to lightly exudating wounds. DuoDERM" Extra Thin dressings are particularly suitable in areas subject to friction and those requiring contouring, e.g., elbows, heels. DuoDERM" Extra Thin dressings interact with wound moisture producing a soft mass that enables removal of the dressing with little or no damage to newly formed tissues. They help isolate the wound against bacterial and other external contamination. INDICATIONS " Management of superficial, dry to lightly exudating dermal ulcers. " Post-operative wounds. " Protective dressings. — Reason: Wound dressing may have foreign matter on the product. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves. 10 drops/mL, 96-inch (2.4 meters). Non-DEHP, Product Code 2R8519 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable Collar, 7.9-inch (20 centimeters), Product Code 2C8634 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoNortheast Scientific Inc. device recall (Cls II)

    NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-152. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US. — Reason: Potential for breaches in the sterile barrier packaging, compromising sterility assurance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 29, 2025device recall350d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

    CLEARLINK SYSTEM Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, 10 drops/mL, 100-inch (2.5 meters), Product Code 2C8425 — Reason: IV sets may leak. — Status: Ongoing

    full page →fda device recalls ↗

    Week of Sep 1, 2025

    12
    ›Sep 2, 2025approval346d agoEPYSQLI (ECULIZUMAB-AAGH) — FDA approvalEPYSQLI

    Sponsor: SAMSUNG BIOEPIS CO LTD. Form: INJECTION. Route: SOLUTION

    full page →EPYSQLI →fda approvals ↗
    ›Sep 2, 2025device 510k
    ← prev
    page 12 of 365
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    346d ago
    Belport Company, Inc., Gingi-Pak — RODIN Cement (510k cleared)

    Product code: EMA. Advisory committee: Dental. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 2, 2025device 510k346d agoChengdu Besmile Medical Technology Co., Ltd. — Customized Abutment and Screw (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 2, 2025device 510k346d agoAerogen, Ltd. — Aerogen Pro-X1 Controller System (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 2, 2025device 510k346d agoPhilips Medizin Systeme Böblingen GmbH — IntelliVue Patient Monitor 6100 (6100); IntelliVue Patient Monitor 6300 (6300); IntelliVue Patient Monitor 6500 (6500) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 2, 2025device 510k346d agoNaitive Technologies, Ltd. — OsteoSight™ Hip (v1) (510k cleared)TAT TECHNOLOGIES LTD

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

    full page →fda device 510k ↗
    ›Sep 2, 2025device 510k346d agoVelmeni, Inc. — VELMENI for DENTISTS (V4D) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 2, 2025device 510k346d agoIgnite Orthomotion — Achieve Partial Knee System - Porous Coated CoCrMo Femoral Component (510k cleared)

    Product code: NJD. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 2, 2025device pma346d agoBoston Scientific Corp — Opal HDx Ablation Connection Box (Maestro); Opal HDx Ablation Connection Box - IntellaNav StablePoint; Opal HDx Ablation (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Sep 2, 2025device pma346d agoJohnson & Johnson Surgical Vision, Inc. — TECNIS™ Toric II 1-Piece IOLs, ZCU TECNIS Symfony Toric II Extended Range of Vision IOLs, ZXU TECNIS Eyhance Toric II IO (PMA supplement)JOHNSON & JOHNSON

    Supplement type: 30-Day Notice. Product code: HQL. Advisory committee: OP. Decision: OK30

    full page →fda device pma ↗
    ›Sep 2, 2025device pma346d agoCochlear Americas — Cochlear™ Nucleus® System (PMA supplement)

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

    full page →fda device pma ↗
    ›Sep 2, 2025device pma346d agoJohnson & Johnson Surgical Vision, Inc. — TECNIS 3-Piece Acrylic Monofocal, Model ZA9003 (PMA supplement)JOHNSON & JOHNSON

    Supplement type: 30-Day Notice. Product code: HQL. Advisory committee: OP. Decision: OK30

    full page →fda device pma ↗
    $FMS23.92+0.84%
    $MDT91.10+0.37%
    $MDT91.10+0.37%
    $TATT
    $BSX51.39-0.07%
    $JNJ261.53+0.26%
    $JNJ261.53+0.26%