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20,185 catalysts · 4,728 grant · 3,126 8k filing · 3,102 device 510k · 2,791 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • 8k filing3,126
  • device 510k3,102
  • approval2,791
  • device pma2,000
  • device recall2,000
device adverse event
1,000
  • recall773
  • earnings583
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of May 19, 2025

    50
    ›May 19, 2025approval450d agoZUBSOLV (BUPRENORPHINE HYDROCHLORIDE) — FDA approvalEdenbridge Pharmaceuticals LLC

    Sponsor: EDENBRIDGE PHARMS. Form: TABLET. Route: SUBLINGUAL

    full page →fda approvals ↗
    ›May 19, 2025device 510k450d agoRowpar Pharmaceuticals, Inc. — CloSYS® Dry Mouth Sensitive Mouth Rinse (510k cleared)RVL Pharmaceuticals Inc

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

    full page →fda device 510k ↗
    ›May 19, 2025device 510k450d agoSplintek, Inc. — SleepRight Snore Aid (510k cleared)

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

    full page →fda device 510k ↗
    ›May 19, 2025device 510k450d agoRoute 92 Medical, Inc. — Route 92 Medical HiPoint Reperfusion System and Aspiration Tubing Set (510k cleared)

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

    full page →fda device 510k ↗
    ›May 19, 2025device 510k450d agoNanjing Perlove Medical Equipment Co., Ltd. — Diagnostic X-ray System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 19, 2025device 510k450d agoGigaalaser Company , Ltd. — Medical Diode Laser Systems (VELAS II-30B, VELAS II-30A, GBOX-15AB, GBOX-20B, CHEESE II-10B) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 19, 2025device 510k450d agoDoc Brands, Inc. — Dentemp Pro-Comfort Dental Guard (510k cleared)BT Brands, Inc.

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

    full page →fda device 510k ↗
    ›May 19, 2025device 510k450d agoBecton, Dickinson and Company — BD Phoenix™ Automated Microbiology System - GN Imipenem-relebactam (0.0625/4 - 16/4 µg/mL) (510k cleared)BECTON DICKINSON & CO

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

    full page →fda device 510k ↗
    ›May 19, 2025device 510k450d agoShenzhen Mindray Bio-Medical Electronics Co., Ltd. — Diagnostic Ultrasound System (Recho R9W); Diagnostic Ultrasound System (Recho R9); Diagnostic Ultrasound System (Recho R9 Pro); Diagnostic Ultrasound System (Recho R9 Exp); Diagnostic Ultrasound System (Recho R9S); Diagnostic Ultrasound System (Recho R9T); Diagnostic Ultrasound System (Crius R9 CV); Diagnostic Ultrasound System (Anesus R9 CV); Diagnostic Ultrasound System (Recho R9 Super); Diagnostic Ultrasound System (Recho R9 Lumi); Diagnostic Ultrasound System (Recho R CV); Diagnost (510k cleared)

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

    full page →fda device 510k ↗
    ›May 19, 2025device 510k450d agoVision Rt, Ltd. — MapRT (510k cleared)Rail Vision Ltd.

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

    full page →fda device 510k ↗
    ›May 19, 2025device 510k450d agoZhengzhou PZ Laser Slim Technology Co., Ltd. — Muscle Stimulator Device (PZ-100) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 19, 2025device 510k450d agoResmed Pty , Ltd. — AirFit F20 Mask System; AirFit F20 NM Mask System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 19, 2025device 510k450d agoRestor3D — restor3d Reverse Total Shoulder Arthroplasty System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 20, 2025approval449d agoAMJEVITA (ADALIMUMAB-ATTO) — FDA approvalAMJEVITA

    Sponsor: AMGEN INC. Form: INJECTABLE. Route: INJECTION

    full page →AMJEVITA →fda approvals ↗
    ›May 20, 2025approval449d agoCYLTEZO (ADALIMUMAB-ADBM) — FDA approvalCYLTEZO

    Sponsor: BOEHRINGER INGELHEIM. Form: INJECTABLE. Route: INJECTION

    full page →CYLTEZO →fda approvals ↗
    ›May 20, 2025approval449d agoHYRIMOZ (ADALIMUMAB-ADAZ) — FDA approvalHYRIMOZ

    Sponsor: SANDOZ INC. Form: INJECTABLE. Route: INJECTION

    full page →HYRIMOZ →fda approvals ↗
    ›May 20, 2025device 510k449d agoFlexicare Medical Limited. — ProVu Single Use Video Stylet with Reinforced ET Tube (Size 6.5) (038-995-065U); ProVu Single Use Video Stylet with Reinforced ET Tube (Size 7.0) (038-995-070U); ProVu Single Use Video Stylet with Reinforced ET Tube (Size 7.5) (038-995-075U); ProVu Single Use Video Stylet with Reinforced ET Tube (Size 8.0) (038-995-080U) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 20, 2025device 510k449d agoAidite (Qinhuangdao) Technology Co., Ltd. — Biomic Color Opaque (510k cleared)

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

    full page →fda device 510k ↗
    ›May 20, 2025device 510k449d agoBreas Medical AB — EveryWare (510k cleared)

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

    full page →fda device 510k ↗
    ›May 20, 2025device 510k449d agoExpanding Innovations, Inc. — X-PAC® N-GAGE™ Lumbar Plate System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 20, 2025device 510k449d agoABBOTT MEDICAL — ViewFlex™ X ICE Catheter, Sensor Enabled™ (510k cleared)

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

    full page →fda device 510k ↗
    ›May 20, 2025device 510k449d agoFujifilm Corporation — SCENARIA View Phase 5.0 (510k cleared)Fujifilm Holdings Corp

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

    full page →fda device 510k ↗
    ›May 20, 2025device 510k449d agoMet One Technologies, LLC — Sovereign Posterior Cervical System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 20, 2025device 510k449d agoMedtronic, Inc. — VitalFlow Console (510k cleared)Medtronic plc

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

    full page →fda device 510k ↗
    ›May 20, 2025device 510k449d agoKeystone Industries — FP3D (510k cleared)

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

    full page →fda device 510k ↗
    ›May 21, 2025approval448d agoHADLIMA (ADALIMUMAB-BWWD) — FDA approvalHADLIMA

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

    full page →HADLIMA →fda approvals ↗
    ›May 21, 2025approval448d agoHADLIMA (ADALIMUMAB-BWWD) — FDA approvalHADLIMA

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

    full page →HADLIMA →fda approvals ↗
    ›May 21, 2025approval448d agoYUFLYMA (ADALIMUMAB-AATY) — FDA approvalYUFLYMA

    Sponsor: CELLTRION. Form: INJECTABLE. Route: INJECTION

    full page →YUFLYMA →fda approvals ↗
    ›May 21, 2025approval448d agoYUFLYMA (ADALIMUMAB-AATY) — FDA approvalYUFLYMA

    Sponsor: CELLTRION. Form: INJECTABLE. Route: INJECTION

    full page →YUFLYMA →fda approvals ↗
    ›May 21, 2025recall448d agoL'Oreal USA recall (Cls II)Galderma Laboratories LP

    La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, a) UPC 3606000508804, 20 mL (0.7 fl. oz.) Tube per Carton, b) 883140500759, 40 mL (1.35 fl. oz.) Tube per Carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, France. — Reason: cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots. — Status: Ongoing

    full page →fda recalls ↗
    ›May 21, 2025recall448d agoL'Oreal USA recall (Cls II)Galderma Laboratories LP

    La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne System, 3 Step Acne Routine Kit, Medicated Gel Cleanser 3.4 fl. oz. (100 mL) Tube, Clarifying Solution 3.4 fl. oz. (100 mL) Tube, Dual Action Acne Treatment 0.7 fl. oz. (20 mL: UPC 883140035275) Tube, (benzoyl peroxide 0.5% and benzoyl peroxide 5.5% and salicylic acid 2%), La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, France, UPC 883140035282 (kit). — Reason: cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots. — Status: Ongoing

    full page →fda recalls ↗
    ›May 21, 2025recall448d agoL'Oreal USA recall (Cls II)Galderma Laboratories LP

    La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, 40 mL (135 FL. OZ.) Tube per carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, Laboratoire Dermatologique, CAI 86270, La Roche-Posay, France, UPC 883140500759. — Reason: Chemical Contamination: This recall has been initiated due to detected trace levels of benzene. — Status: Ongoing

    full page →fda recalls ↗
    ›May 21, 2025recall448d agoEmpower Clinic Services, LLC dba Empower Pharmacy recall (Cls II)Slayback Pharma LLC

    Testosterone Cypionate Injection, 200 mg/mL, CIII, Rx Only, 5 mL Sterile Multiple-Dose Vial, Compounded by: Empower Pharmacy, 7601 N Sam Houston Pkwy W Ste 100, Houston, TX, 77064, Phone: (877) 562-8577, Compounding Date: 08/20/2024, Beyond Use by Date: 05/28/2025, Lot 202364. — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›May 21, 2025device 510k448d agoShanghai United Imaging Healthcare Co., Ltd. — uMR Omega (510k cleared)

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoMem Dental Technology Co., Ltd. — MEM Clear Aligner System (510k cleared)Meiwu Technology Co Ltd

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoFujifilm Corporation — Synapse 3D Base Tools (V7.0) (510k cleared)Fujifilm Holdings Corp

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoRay Co., Ltd. — SMARTDent (510k cleared)Ray Therapeutics Inc

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoIntegrity Implants Inc. Dba Accelus — FlareHawk Interbody Fusion System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoSpinal Elements, Inc. — The Karma® Fixation System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoVoco GmbH — GrandioSO Unlimited (510k cleared)

    Product code: EBF. Advisory committee: Dental. Type: Special

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoStryker Endoscopy — Stryker AlphaVent™ Knotless SP Biocomposite Anchor (510k cleared)

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoHyperfine, Inc. — Swoop® Portable MR Imaging® System (510k cleared)Hyperfine, Inc.

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoPrintbio, Inc. — 3DMatrix DynaFlex (DynaFlex) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoHjy Smart Medical Device Co., Ltd. — HJY VisualNext 3D Endoscopic Vision System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoTandem Diabetes Care, Inc. — Control-IQ+ technology (510k cleared)TANDEM DIABETES CARE INC

    Product code: QJI. Advisory committee: Clinical Chemistry. Type: Traditional

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoFinemedix Co., Ltd. — ClearHemograsper (510k cleared)

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoPhilips Ultrasound, LLC — EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoInVision Medical Technology Corporation — InVision Precision Cardiac Amyloid (510k cleared)

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoAnx Robotica Corporation — MotiliCap GI Monitoring System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 21, 2025device 510k448d agoAlma Lasers, Inc. — The Alma Hybrid Laser System (510k cleared)

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

    full page →fda device 510k ↗
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    $HYPR
    $TNDM23.44+2.76%
    $AMGN414.03-0.76%
    $WNW
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