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23,664 catalysts · 5,000 device 510k · 4,728 grant · 3,915 approval · 3,230 8k filing · 2,000 device pma · 2,000 device recall

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  • device 510k5,000
  • grant4,728
  • approval3,915
  • 8k filing3,230
  • device pma2,000
  • device recall2,000
recall
1,126
  • device adverse event1,000
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Nov 4, 2024

    50
    ›Nov 4, 2024device 510k648d agoComercializadora Brever — CDB Hospital ® Sterilization Wrap (70 gsm); CDB Hospital ® Sterilization Wrap (44 gsm) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 5, 2024approval647d agoDEFLAZACORT — FDA approvalAmneal Pharmaceuticals, Inc.

    Sponsor: UPSHER SMITH LABS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 5, 2024device 510k647d agoKyocera Medical Technologies, Inc. — Skyway Anterior Cervical Plate System (510k cleared)Medical Care Technologies Inc.

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

    full page →fda device 510k ↗
    ›Nov 5, 2024device 510k647d agoFirst Medical Source, LLC — InfuLife (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 5, 2024device 510k647d agoTerrats Medical SL — DESS Dental Smart Solutions (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 5, 2024device 510k647d agoQuantalx Neuroscience — Delphi Stimulator (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 5, 2024device 510k647d agoShenzhen Kentro Medical Electronics Co., Ltd. — Transcutaneous Electronic Nerve Stimulator (KTR-2301, KTR-2302, KTR-2341, KTR-2342, KTR-2401, KTR-2402, KTR-2411, KTR-2412, KTR-2491, KTR-2492, KTR-2493, KTR-2494) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 5, 2024device 510k647d agoImaxeon Pty, Ltd. — MEDRAD Centargo CT Injection System; MEDRAD Centargo Day Set; MEDRAD Centargo Patient Line; MEDRAD Centargo Replacement Spike; MEDRAD ISI2 Module (ISI2) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 5, 2024device 510k647d agoGri-Alleset, Inc. — gentleheel® Adult Incision Device (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 5, 2024device 510k647d agoOrthopedic Designs North America, Inc. (Odi-Na) — Atlas™ Humeral Nail System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 5, 2024device 510k647d agoJeisys Medical, Inc. — POTENZA (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 5, 2024device 510k647d agoCardio Flow Inc., — FreedomFlow™ Orbital Circumferential Atherectomy System (510k cleared)

    Product code: MCW. Advisory committee: Cardiovascular. Type: Special

    full page →fda device 510k ↗
    ›Nov 5, 2024device 510k647d agoTerarecon,Inc. — TeraRecon Cardiac.Chambers.MR (1.0.0) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 5, 2024device 510k647d agoCarboFix Orthopedics , Ltd. — CarboClear® Hybrid Pedicle Screw System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 6, 2024recall646d agoBLI International, Inc. recall (Cls II)ICF International, Inc.

    Chlorpheniramine Maleate 4 mg tablets, 24-count bottle, Manufactured For: Athlete's Needs, Novi, MI 48377, NDC 53185-277-24 — Reason: Superpotent Drug: Stability failure for assay at 6 months test time-point. — Status: Terminated

    full page →fda recalls ↗
    ›Nov 6, 2024recall646d agoACCORD HEALTHCARE, INC. recall (Cls II)HCA Healthcare, Inc.

    Cinacalcet Tablets, 90 mg, Rx Only, a) 30 Tablets per bottle, NDC: 16729-442-10, b) 90 Tablets per bottle, NDC: 16729-442-15, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703. Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad - 382 210, INDIA. — Reason: CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 6, 2024recall646d agoDr. Reddy's Laboratories, Inc. recall (Cls II)DR REDDYS LABORATORIES LTD

    Cinacalcet Tablets, 90 mg, 30-count bottle, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India., NDC 43598-369-30. — Reason: CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 6, 2024recall646d agoACCORD HEALTHCARE, INC. recall (Cls II)HCA Healthcare, Inc.

    Cinacalcet Tablets, 60 mg, Rx Only, a) 30 Tablets per bottle, NDC: 16729-441-10, b) 90 Tablets per bottle, NDC: 16729-441-15, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703. Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad - 382 210, INDIA. — Reason: CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 6, 2024recall646d agoDr. Reddy's Laboratories, Inc. recall (Cls II)DR REDDYS LABORATORIES LTD

    Cinacalcet Tablets, 60 mg, 30-count bottles, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India, NDC 43598-368-30. — Reason: CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 6, 2024recall646d agoACCORD HEALTHCARE, INC. recall (Cls II)HCA Healthcare, Inc.

    Cinacalcet Tablets 30 mg, Rx Only, a) 30 Tablets per bottle, NDC: 16729-440-10, b) 90 Tablets per bottle, NDC: 16729-440-15, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703, Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad - 382 210, INDIA. — Reason: CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 6, 2024recall646d agoDr. Reddy's Laboratories, Inc. recall (Cls II)DR REDDYS LABORATORIES LTD

    Cinacalcet Tablets, 30 mg, 30-count bottle, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India, NDC 43598-367-30. — Reason: CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 6, 2024device 510k646d agoNu Eyne Co., Ltd. — ELEXIR 2.0 (ALLIVE3) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 6, 2024device 510k646d agoAcuitive Technologies, Inc. — Citrepore™ (510k cleared)Aeva Technologies, Inc.

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

    full page →fda device 510k ↗
    ›Nov 6, 2024device 510k646d agoBiofire Diagnostics, LLC (Biomerieux) — BIOFIRE® FILMARRAY® Pneumonia Panel (BIOFIRE Pneumonia Panel); BIOFIRE® FILMARRAY® Pneumonia Panel plus (BIOFIRE Pneumonia Panel plus) (510k cleared)

    Product code: QDS. Advisory committee: Pathology. Type: Special

    full page →fda device 510k ↗
    ›Nov 6, 2024device 510k646d agoMedtech Products, Inc. — Compound W Skin Tag Remover (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 6, 2024device 510k646d agoBiotech Dental, LLC — Accelx Implant System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 6, 2024device 510k646d agoAsclepion Laser Technologies GmbH — MultiCut Solo (510k cleared)

    Product code: GCJ. Advisory committee: Gastroenterology, Urology. Type: Special

    full page →fda device 510k ↗
    ›Nov 6, 2024device 510k646d agoMedisurge, LLC — Agility Symmetric™ Total Knee System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 6, 2024device 510k646d agoShenzhen Ulike Smart Electronics Co., Ltd. — Ice Cooling IPL Hair Removal Device (UIM20 GR, UIM20 BK, UIM20 SL, UIM20 CB, UIM20 WR) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 6, 2024device 510k646d agoABBOTT MEDICAL — Hi-Torque Command 14 ST Guide Wire and Hi-Torque Command 14 MT Guide Wire (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024approval645d agoDANZITEN (NILOTINIB TARTRATE) — FDA approvalDANZITEN

    Sponsor: AZURITY. Form: TABLET. Route: ORAL

    full page →DANZITEN →fda approvals ↗
    ›Nov 7, 2024approval645d agoPIFELTRO (DORAVIRINE) — FDA approvaldoravirine

    Sponsor: MSD MERCK CO. Form: TABLET. Route: ORAL

    full page →doravirine →fda approvals ↗
    ›Nov 7, 2024approval645d agoDELSTRIGO (DORAVIRINE) — FDA approval(doravirine + lamivudine + tenofovir disoproxil fumarate)

    Sponsor: MSD MERCK CO. Form: TABLET. Route: ORAL

    full page →(doravirine + lamivudine + tenofovir disoproxil fumarate) →fda approvals ↗
    ›Nov 7, 2024device 510k645d agoExostat Medical, Inc. — MicroTrend System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoInrad, Inc. — Trilogy Tissue Marker (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoSpident Co., Ltd. — VioSeal (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoRebotix — Remanufactured EndoWrist ProGrasp Forceps (420093) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoNeurocareai, Inc. — NeuroICH (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoVarian Medical Systems, Inc. — Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve (510k cleared)MERIT MEDICAL SYSTEMS INC

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoStryker Spine — OZARK Cervical Plate System; PYRENEES® Cervical Plate System; EVEREST® Spinal System; MESA® Spinal System; MESA® Small Stature Spinal System; CASPIAN® Spinal System; DENALI® Spinal System; DENALI® MI Spinal System; YUKON OCT Spinal System; Xia® 3 Spinal System; K2M Patient Specific; CASCADIA™ Interbody System; CAYMAN® Plate System; CAYMAN® Plate System-MI (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoAspen Imaging Healthcare, Inc. — IODR1717 / IODR1417 / IODR1417-GF (Digital Flat Panel X-ray Detector) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoBiofire Diagnostics, LLC — BIOFIRE FILMARRAY Gastrointestinal (GI) Panel (510k cleared)

    Product code: PCH. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoZsfab — ZSFab Cervical Interbody System; ZSFab Lumbar Interbody System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoOssvis Co., Ltd. — LL Implant System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoShenzhen Greatro Electronic Technology Co., Ltd. — Intense Pulse Light Therapeutic Apparatus (IPL-18 BF, IPL-18 FG) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoFoundation Surgical Group, Inc. — Vertiwedge® Intraosseous System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoMako Surgical Corp. — Mako Shoulder Application (1.0) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoIcometrix NV — icobrain aria (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 7, 2024device 510k645d agoNewclip Technics — Newclip Patient-matched instrumentation non sterile PSI (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 8, 2024approval644d agoOMEPRAZOLE — FDA approvalomeprazole DR

    Sponsor: DEXCEL PHARMA. Form: TABLET, DELAYED RELEASE. Route: ORAL

    full page →omeprazole DR →fda approvals ↗
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    $RDY12.38-0.08%
    $MDCE0.00020.00%
    $ICFI89.58-1.10%
    $HCA407.07-1.81%
    $HCA407.07-1.81%
    $AMRX17.66+3.27%
    $MRK134.79+1.41%
    $HCA407.07-1.81%
    $AEVA
    $RDY12.38-0.08%
    $MRK134.79+1.41%
    $RDY12.38-0.08%
    $MMSI90.72-0.53%