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calendar

13,623 catalysts · 3,603 8k filing · 2,401 grant · 2,100 approval · 1,445 device 510k · 1,074 device recall · 1,000 device adverse event

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  • 8k filing3,603
  • grant2,401
  • approval2,100
  • device 510k1,445
  • device recall1,074
  • device adverse event1,000
device pma
959
  • earnings585
  • recall376
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Dec 22, 2025

    50
    ›Dec 23, 2025device 510k250d agoHycor Biomedical — NOVEOS Specific IgE (sIgE); Capture Reagent F024, Shrimp (Shrimp spp.); Capture Reagent F207, Clam (Mercenaria mercenaria); Capture Reagent F256, Walnut (Juglans spp.) ; Capture Reagent I006, German Cockroach (Blatella germanica) (510k cleared)Dawn Sea Therapeutics

    Product code: DHB. Advisory committee: Immunology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoCylite Pty. , Ltd. — UNITY DX (UDX) (510k cleared)

    Product code: OBO. Advisory committee: Ophthalmic. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoPhilips Consumer Lifestyle B.V. — Philips Lumea IPL (510k cleared)

    Product code: OHT. Advisory committee: General, Plastic Surgery. Type: Special

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoSignature Orthopaedics Pty, Ltd. — Active-V Total Knee System; World Total Knee System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoHong Qiangxing (Shenzhen) Electronics Limited — TENS&EMS (HZ9151B, HZ9151C, HZ9151D) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoOrangecad Med GmbH — OrangeCAD Med Abutments (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoDynapulse Medical — VEINOPLUS Back (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoAura Medical, LLC — Aura Glide (FC40) (510k cleared)QOL Medical LLC

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoBruno Vision Care, LLC — Deseyne (vifilcon C) Daily Disposable Soft (hydrophilic) Contact Lens with UV Blocking for Presbyopia (EDOF) (510k cleared)

    Product code: LPL. Advisory committee: Ophthalmic. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoDongguan Yijiaming Technology Co., Ltd. — LED Light Therapy Device (HLGMZ-3W-G1V1,HLGMZ-3W-G2V1,HLG-GJXJ-G1V1,HGMZ-2W-G1V1, HGMZ-2W-G2V1,MRD-GJXJ-G1V1.) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoGe Medical Systems, LLC — AIR Recon DL (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoLinhejiacheng (Shenzhen) E-Commerce Co., Ltd. — Paruu Wearable Breast pump (P16, P16-A, P16-B, P16-C, P16-D, P20, P9, P10, P10 PRO, P21, P22, P23, P24, P25, P26, P27, P28, P29, P30, P20-A, P20-B, P20-C, P20-D) (510k cleared)

    Product code: HGX. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoMedimaging Integrated Solution, Inc (Miis) — MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoGuangdong Prestige Technology Co., Ltd. — Electric Scooter (S202572J, S2060, M2089, S2050) (510k cleared)

    Product code: INI. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoParagon Implant Mfg., LLC — NizPlant Dental Implant System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoHai Solutions — QIKCAP System (510k cleared)

    Product code: SGX. Advisory committee: General Hospital. Type: Direct

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoShenzhen Safesecure Medical Infection Control Tech Co. , Ltd. — SafeSecure Steam Sterilization Process Indicator (4012, 4013, 4014, 4016); SafeSecure Vaporized Hydrogen Peroxide Sterilization Process Indicator (4211, 4212, 4213) (510k cleared)Kortuc Japan LLC

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoEdan Instruments, Inc. — Diagnostic Ultrasound System (Nano C5, Nano C5 EXP, Nano L12, and Nano L12 EXP) (510k cleared)VEECO INSTRUMENTS INC

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoHealgen Scientific,, LLC — Healgen Accurate Urine Drug Screen Dip Card; Healgen Accurate Home Urine Drug Test Dip Card (510k cleared)

    Product code: NGL. Advisory committee: Clinical Toxicology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoDiaSorin, Inc. — LIAISON® XL MUREX Anti-HDV (318260); LIAISON® XL MUREX Control Anti-HDV (318261) (510k cleared)Dawn Sea Therapeutics

    Product code: SGW. Advisory committee: Immunology. Type: Direct

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoParagon Implant Mfg., LLC — GEN5™ and GEN5+™ 3.3mmD Dental Implants (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoMedentika GmbH — Custom Abutments AS (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoTherapanacea Sas — ART-Plan+ (v3.1.0) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoSim&Cure — Sim&Size (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device 510k250d agoOsteoremedies, LLC — OsteoRemedies Hip Spacer System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2025device pma250d agoABBOTT MEDICAL — Infinity™ Deep Brain Stimulation (DBS) System (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoMesoblast — SYNOJOYNT™ (PMA supplement)MESOBLAST LTD

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoABBOTT MEDICAL — Proclaim™ Spinal Cord Stimulation (SCS) System (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoMedtronic Neuromodulation — InterStim™ Therapy System, Verify™ Evaluation System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: QON. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoQ-Med AB — Restylane® Lyft with Lidocaine (PMA supplement)Sustained Therapeutics Inc

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoRayner Intraocular Lenses , Ltd. — C-FLEX MODEL 570C INTRAOCULAR LENS (IOL) (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoBioventus, LLC — DUROLANE (PMA supplement)Bioventus Inc.

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoCooperVision, Inc. — MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoSt Jude Medical — TactiCath™ Contact Force Ablation Catheter, Sensor Enabled™ (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoABBOTT MEDICAL — Amplatzer™ Amulet™ Left Atrial Appendage Occluder (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoMedtronic Neuromodulation — InterStim™ Therapy System, Verify™ Evaluation System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: EZW. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoVantive US Healthcare, LLC — Gambro Prismaflex TPE 2000 Set (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MDP. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoBiosense Webster, Inc. — TRUPULSE™ Generator (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoBiosense Webster, Inc. — nGEN™ Pump (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoABBOTT MEDICAL — Proclaim Dorsal Root Ganglion (DRG) System (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 23, 2025device pma250d agoEndologix, LLC — DETOUR System (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 23, 2025device recall250d agoFocalyx Technologies, LLC. device recall (Cls II)

    Focalyx Fusion — Reason: Software device that is an accessory for image-guided interventional and diagnostic procedures involving prostate has accessories that may not function properly with Windows 10, which may cause patient harm during biopsy or cause treatment/therapy delays, so firm is recommending stop use until device is verified/validated with Windows 11. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 23, 2025device recall250d agoBeckman Coulter, Inc. device recall (Cls II)

    CellMek SPS Sample Preparation System, REF: C44603, with software — Reason: Sample preparation system designed to automate staining, lysing, cell washing has a software error that causes samples to be dispensed close to or touching tube bottoms, which could dislodge fluid line, result in sample loss, spillage, make instrument inoperable and will lead to unintentional removal of 60-100 microliters from final sample, may lead to incorrect diagnosis or patient management. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 24, 2025approval249d agoCHILDREN'S ZYRTEC HIVES (CETIRIZINE HYDROCHLORIDE) — FDA approvalKenvue Inc.

    Sponsor: KENVUE BRANDS. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Dec 24, 2025recall249d agoGolden State Medical Supply Inc. recall (Cls II)Beximco Pharmaceuticals USA Inc

    Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporated, CA 93012 USA. NDC 51407-973-10 — Reason: Presence of Foreign Tablets/Capsules — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 24, 2025recall249d agoSUN PHARMA /TARO recall (Cls II)ATLAS Molecular Pharma SL

    Ciclopirox Shampoo, 1%, 120 mL, Rx only, Mfg by: Taro Pharmaceuticals Inc., Ontario, Canada; Dist. by: Taro Pharmaceuticals USA, Inc., NY 10532. NDC 51672-1351-08 — Reason: Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 24, 2025recall249d agoSOMERSET THERAPEUTICS LLC recall (Cls III)Somerset Therapeutics LLC

    Cisatracurium Besylate Injection USP, 20 mg/10 mL*,(2 mg/mL), 10 x 10 mL Multiple-dose Vials per carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, 10mL Multiple-dose vial, NDC 70069-161-01; 10x10mL Multiple-dose vials per Carton, NDC 70069-161-01. — Reason: Subpotent product:out of specification assay results observed during long term stability testing. — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 24, 2025recall249d agoNovocol Pharmaceutical of Canada, Inc. recall (Cls II)

    Benco dental Graham CHEMICAL CO., Mepivacaine HCI 3% (30 mg/mL) Injection, [Mepivacaine HCI Injection, USP], packaged in a carton containing 50 single-dose Cartridges, 1.7 mL each, Rx only, Distributed by Benco Dental 295 Center Point Blvd, Pittston, PA 18640, Manufactured by Novocol Pharmaceutical of Canada, Inc., NDC 66975-406-51. — Reason: Defective container: cracked/broken cartridges — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 24, 2025recall249d agoPreferred Pharmaceuticals, Inc. recall (Cls II)InMed Pharmaceuticals Inc.

    Ondansetron ODT Tablets, USP 4mg, 1x10 unit dose tablets, Mfg: Glenmark Pharmaceuticals Limited, Repackaged by Preferred Pharmaceuticals NDC 68788-8666-01 — Reason: Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out. Preferred Pharmaceuticals purchased the finished product and repackaged the product for sale. — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 24, 2025recall249d agoNovocol Pharmaceutical of Canada, Inc. recall (Cls II)

    darby dental supply, MEPIVACAINE, Mepivacaine HCI 3% (30mg/mL) Injection, [Mepivacaine HCI Injection, USP], packaged in a carton containing 50 single-dose Cartridges, 1.7 mL each, Rx only, Manufactured by Novocol Pharmaceutical of Canada, Inc., NDC 66467-9760-5. — Reason: Defective container: cracked/broken cartridges — Status: Ongoing

    full page →fda recalls ↗
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    $KVUE19.20-0.10%
    $BVS8.6700+1.40%
    $MESO18.18+7.96%
    $VECO59.42+2.95%
    $INM1.3800-3.50%