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calendar

20,468 catalysts · 4,728 grant · 3,312 device 510k · 3,086 8k filing · 2,841 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • device 510k3,312
  • 8k filing3,086
  • approval2,841
  • device pma2,000
  • device recall2,000
device adverse event
1,000
  • recall836
  • earnings583
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Apr 14, 2025

    8
    ›Apr 18, 2025device 510k481d agoAllengers Medical Systems Limited — Wireless/ Wired X-Ray Flat Panel Detectors (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 18, 2025device 510k481d agoSEKISUI Diagnostics, LLC — Acucy® Influenza A&B Test with the Acucy® 2 System (510k cleared)

    Product code: PSZ. Advisory committee: Microbiology. Type: Dual Track

    full page →fda device 510k ↗
    ›Apr 18, 2025device 510k481d agoiSMART Developments, Ltd. — handLITE (TN19S) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 18, 2025device 510k481d agoZimmer Biomet — Zimmer Biomet Ceramic Heads (22.2mm diameter) (510k cleared)ZIMMER BIOMET HOLDINGS, INC.

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

    full page →fda device 510k ↗
    ›Apr 18, 2025device 510k481d agoTechnoflex Sas. — DMRX 100ml Empty Container Solution; DMRX 250ml Empty Container Solution; DMRX 500ml Empty Container Solution; DMRX 1000ml Empty Container Solution (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 18, 2025device 510k481d agoLuminex Corporation — LIAISON PLEX Gram-Negative Blood Culture Assay (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 18, 2025device 510k481d agoTamabio — PeriBeam® Pericardial Membrane (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 18, 2025device 510k481d agoSKY Medical, a.s. — Extension Feeding Set with ENFit™ Connectors (510k cleared)

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

    full page →fda device 510k ↗

    Week of Apr 21, 2025

    42
    ›Apr 21, 2025approval478d agoKEYTRUDA (PEMBROLIZUMAB) — FDA approvalpembrolizumab

    Sponsor: MERCK SHARP DOHME. Form: SOLUTION. Route: INTRAVENOUS

    full page →pembrolizumab →fda approvals ↗
    ›Apr 21, 2025approval
    ← prev
    page 5 of 410
    next →
    478d ago
    MEKINIST (TRAMETINIB DIMETHYL SULFOXIDE) — FDA approvalSpexotras

    Sponsor: NOVARTIS. Form: TABLET. Route: ORAL

    full page →Spexotras →fda approvals ↗
    ›Apr 21, 2025device 510k478d agoEc Certification Service GmbH — Composite Orthodontic Brackets and Buttons (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 21, 2025device 510k478d agoAsahi Intecc Co., Ltd. — CHIKAI Nexus 014 (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 21, 2025device 510k478d agoShenzhen TPH Technology Co., Ltd. — Wearable breast pump (model S12A) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

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

    full page →fda device 510k ↗
    ›Apr 21, 2025device 510k478d agoD.A.N.D. Metal Industries North, Ltd. — DAND Dental Implant System (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 21, 2025device 510k478d agoGE Medical Systems SCS — VersaViewer (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 21, 2025device 510k478d agoDk Medical Technology Co., Ltd. — D·Kutting™ LL Peripheral Scoring Balloon Dilatation Catheter (510k cleared)NewBay Medical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›Apr 21, 2025device 510k478d agoSpectrum Antimicrobials, Inc. — Spectricept Skin and Wound Cleanser (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 22, 2025approval477d agoTEVIMBRA (TISLELIZUMAB-JSGR) — FDA approvalBeOne Medicines Ltd.

    Sponsor: BEIGENE. Form: INJECTION. Route: SOLUTION

    full page →fda approvals ↗
    ›Apr 22, 2025approval477d agoTEVIMBRA (TISLELIZUMAB-JSGR) — FDA approvalBeOne Medicines Ltd.

    Sponsor: BEIGENE. Form: INJECTION. Route: SOLUTION

    full page →fda approvals ↗
    ›Apr 22, 2025approval477d agoTEVIMBRA (TISLELIZUMAB-JSGR) — FDA approvalBeOne Medicines Ltd.

    Sponsor: BEIGENE. Form: INJECTION. Route: SOLUTION

    full page →fda approvals ↗
    ›Apr 22, 2025approval477d agoTEVIMBRA (TISLELIZUMAB-JSGR) — FDA approvalBeOne Medicines Ltd.

    Sponsor: BEIGENE. Form: INJECTION. Route: SOLUTION

    full page →fda approvals ↗
    ›Apr 22, 2025approval477d agoTEVIMBRA (TISLELIZUMAB-JSGR) — FDA approvalBeOne Medicines Ltd.

    Sponsor: BEIGENE. Form: INJECTION. Route: SOLUTION

    full page →fda approvals ↗
    ›Apr 22, 2025approval477d agoTEVIMBRA (TISLELIZUMAB-JSGR) — FDA approvalBeOne Medicines Ltd.

    Sponsor: BEIGENE. Form: INJECTION. Route: SOLUTION

    full page →fda approvals ↗
    ›Apr 22, 2025device 510k477d agoMedtronic Sofamor Danek USA, Inc. — Adaptix™ Interbody System with Titan nanoLOCK™ Surface Technology (510k cleared)Medtronic USA Inc

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

    full page →fda device 510k ↗
    ›Apr 22, 2025device 510k477d agoOcusciences, Inc. — OcuMet Beacon (OCUB100) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 22, 2025device 510k477d agoEvoden Indústria Comércio Importação E Exportação — Evoblock, Perléon (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 22, 2025device 510k477d agoJeil Medical Corporation — ARIX Femur Nail System (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 22, 2025device 510k477d agoMedentika GmbH — Medentika CAD/CAM Abutments (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 22, 2025device 510k477d agoGoodman Co., Ltd. — Aperta NSE PTA Balloon Dilatation Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 22, 2025device 510k477d agoAcuity Surgical Devices, LLC — Ventris Intervertebral Body Fusion Device (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 22, 2025device 510k477d agoBd Integrated Diagnostic Solutions/Becton, — BD CTGCTV2 (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 23, 2025recall476d agoDirect Rx recall (Cls II)Bedford Laboratories

    CIPROFLOXACIN OPHTH SOLUTION, 0.3% 5mL bottle, Rx Only, Generic for CILOXAN, Packaged and Distributed by: DIRECT Rx, NDC 61919-795-05. — Reason: Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 23, 2025recall476d agoEugia US LLC recall (Cls II)Eugia US LLC

    Testosterone Cypionate Injection, USP, CIII, 200mg per mL, Rx only, 1mL Single-Dose Vial, Distributed by Eugia US LLC, E. Windsor, NJ, Manufactured by: Eugia Specialties Limited, Telangana State, India, NDC 55150-277-01 — Reason: cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials. — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 23, 2025recall476d agoDr. Reddy's Laboratories, Inc. recall (Cls I)DR REDDYS LABORATORIES LTD

    Levetiracetam 0.75% in Sodium Chloride Injection 1,000 mg/100 mL (10 mg/mL), 1 x 100mL, Rx Only, Manufactured by: Gland Pharma Limited, Hyderabad, - 500 043 INDIA, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, NDC 43598-636-52 — Reason: LABELING: LABEL MIX-UP: The infusion bag is incorrectly labeled as Levetiracetam in 0.82% Sodium Chloride Injection 500 mg/100 mL, while the aluminum overwrap packaging correctly identifies the product as Levetiracetam in 0.75% Sodium Chloride Injection 1,000 mg/100 mL. — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 23, 2025recall476d agoChattem Inc recall (Cls II)Chattem Inc

    Unisom, SleepMinis, Diphenhydramine HCl, Mini-Capsules, 25 mg, 60 Mini-Capsules bottles, Dist. by Chattem, Inc., P.O. Box 2219, Chattanooga, TN 37409-0219, USA, UPC 0 41167 00670 2 — Reason: CGMP Deviations; detection of Nitrosamine Drug Substance-Related Impurities (NDSRI), N-nitroso-desmethyl-diphenhydramine (n-dph), above the FDA Recommended Intake Limit — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 23, 2025recall476d agoThe Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recall (Cls II)Fosun Pharma USA Inc

    ChlorproMAZINE Hydrochloride Tablets, USP, 10 mg, packaged in cartons of 100 TABLETS (10x10), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC 0904-7129-61 — Reason: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 23, 2025device 510k476d agoHycor Biomedical — NOVEOS Specific IgE (sIgE) Assay; Capture Reagent G010, Johnson Grass (Sorghum halepense); Capture Reagent T007, Oak (Quercus alba) ; Capture Reagent G002, Bermuda Grass (Cynodon dactylon); Capture Reagent W001, Common Ragweed (Ambrosia artemisiifolia); Capture Reagent E005, Dog Dander (Canis familiaris); Capture Reagent T003, Common Silver Birch (Betula verrucosa); Capture Reagent F001, Egg White (Gallus gallus); Capture Reagent F002, Cow's Milk (Bos taurus); NOVEOS Immunoassay Analyz (510k cleared)Dawn Sea Therapeutics

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

    full page →fda device 510k ↗
    ›Apr 23, 2025device 510k476d agoShenzhen Kingboom Technology Co., Ltd. — Electric Nasal Aspirator (BC026, BC025, BC023) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

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

    full page →fda device 510k ↗
    ›Apr 23, 2025device 510k476d agoMedacta International S.A. — Mpact 3D Metal Augments II (510k cleared)Stemedica International S.A.

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

    full page →fda device 510k ↗
    ›Apr 23, 2025device 510k476d agoSofradim Production — Parietene™ Macroporous Mesh (PPM5050 ) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 23, 2025device 510k476d agoNewclip Technics — Xpert Knee (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 23, 2025device 510k476d agoGmp Medicare Sdn. Bhd. — Nitrile Powder Free Examination Glove, Blue Tested for Use with 60 Chemotherapy Drugs, Gastric Acid, Xylazine and Fentanyl (510k cleared)NutriBand Inc.

    Product code: LZA. Advisory committee: General Hospital. Type: Special

    full page →fda device 510k ↗
    ›Apr 23, 2025device 510k476d agoLEM Surgical AG — Dynamis Robotic Surgical System (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 23, 2025device 510k476d agoEsonic Technology (Wuhan) Co., Ltd. — eHertz Functional Series Diagnostic Ultrasound System (eHertz C, eHertz E, eHertz R, eHertz S) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 23, 2025device 510k476d agoAnnalise-Ai — Annalise Enterprise (510k cleared)

    Product code: QFM. Advisory committee: Radiology. Type: Special

    full page →fda device 510k ↗
    ›Apr 23, 2025device 510k476d agoSonavex, Inc. — EchoGuide (Version 1) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 23, 2025device 510k476d agoLaon Medi, Inc. — Laon Ortho (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 23, 2025device 510k476d agoMedacta International S.A. — MySpine WebPlanner (510k cleared)Stemedica International S.A.

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

    full page →fda device 510k ↗
    ›Apr 24, 2025approval475d agoALEVE (NAPROXEN SODIUM) — FDA approvalNAPROXEN SODIUM

    Sponsor: BAYER. Form: TABLET. Route: ORAL

    full page →NAPROXEN SODIUM →fda approvals ↗
    ›Apr 24, 2025device 510k475d agoSurGenTec, LLC — ALARA BMA Neuro Access Kit (ALARA BMAN and ALARA BMAC Kit) (510k cleared)

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

    full page →fda device 510k ↗
    $ZBH87.97+0.93%
    $ONC359.00+3.08%
    $ONC359.00+3.08%
    $RDY12.15-0.57%
    $ONC359.00+3.08%
    $ONC359.00+3.08%
    $ONC359.00+3.08%
    $ONC359.00+3.08%
    $NTRB2.9000-11.59%
    $NVS156.79+0.29%
    $FRTRY
    $FRTRY