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20,728 catalysts · 4,728 grant · 3,411 8k filing · 3,266 device 510k · 2,828 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • 8k filing3,411
  • device 510k3,266
  • approval2,828
  • device pma2,000
  • device recall2,000
device adverse event
1,000
  • recall830
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Aug 11, 2025

    50
    ›Aug 13, 2025device recall372d agoBeckman Coulter Inc. device recall (Cls II)

    UniCel DxH 690T COULTER Cellular Analysis System, configured with the Led HGB Photometer REF: C34520 — Reason: Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall372d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT, 362010-1, 370000-1WL, 360010-1L, 360010-1W, 360010-XWTL, 370000-XWL, 360010-1WTL, 360010-XWT, 360010-2, 370000-2W, 360010-2L, 370000-2WL, 360010-X, 370000-XW, 360010-2W, 362010-2, 360010, 37000-XWL, 362010-X, 362010-XL, 362010-1L, 360010-XL, 37000-1W, 360010-XW, 3700000-1W, 362010-2L, 36010-XWT, 370000-1L, 360010-2WT, 360000-1, 360010-XWSB, 360010-XLSB — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall372d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-X — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall372d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 860010-1L — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall372d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall372d agoBeckman Coulter Inc. device recall (Cls II)

    UniCel DxH 600 COULTER Cellular Analysis System, configured with the Led HGB Photometer REF:B23858 — Reason: Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall372d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. Ingenuity CT 728326, Model Number: 728321. 2. Ingenuity CT 728326, Model Number: 728323. 3. Ingenuity CT, Model Number: 728326. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall372d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall372d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. Ingenuity Core128 / Elite China, Model Number: 728324. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall372d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2 — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall372d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. Brilliance iCT SP, Model Number: 728311. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device 510k372d agoBaisheng Medical Co., Ltd. — Electrotherapy Electrodes (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoBruker Daltonics GmbH & Co. KG — MBT Compass HT CA Software; MBT FAST Shuttle US IVD (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoE.M.S Electro Medical Systems S.A — DOLORCLAST Focused Shock Waves (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoUnibeauty (Hubei) Technology Co., Ltd. — Unscented menstrual long applicator tampon; Unscented menstrual Compact Applicator Tampon; Unscented menstrual Cardboard Applicator Tampon; Unscented menstrual Digital Tampons (510k cleared)

    Product code: HEB. Advisory committee: Obstetrics/Gynecology. Type: Special

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoPipeline Medical Products, LLC — AeroJet Ventilation Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoNuwellis, Inc. — Dual Lumen Extended Length Catheter (dELC), 6F, 12cm (320101); Dual Lumen Extended Length Catheter (dELC), 6F, 16 cm (320102) (510k cleared)Nuwellis, Inc.

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoAppliedvr — RelieVRx (Pico G3) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoKarl Storz SE & CO. KG — KARL STORZ HOPKINS Telescopes for Urology (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoUnimed Medical Supplies, Inc. — Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U403-117); Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U103-117); Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U410-121); Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U110-121) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoOsstem Implant Co., Ltd. — Bone Screw (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoS.I.N. Implant System Ltda — S.I.N. Dental Implant System (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoHuizhou Lvb Maternal and Infant Supplies Co., Ltd. — Wearable Breast Pump (P9, P10, P16, P20, P21, P22, P23, P25) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoStryker GmbH — T2 Alpha Femur Retrograde Nailing System (510k cleared)STRYKER CORP

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k372d agoRiverpoint Medical — HS Fiber (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025approval371d agoOTULFI (USTEKINUMAB-AAUZ) — FDA approvalOTULFI

    Sponsor: FRESENIUS KABI USA. Form: INJECTABLE. Route: INJECTION

    full page →OTULFI →fda approvals ↗
    ›Aug 14, 2025approval371d agoOTULFI (USTEKINUMAB-AAUZ) — FDA approvalOTULFI

    Sponsor: FRESENIUS KABI USA. Form: INJECTABLE. Route: INJECTION

    full page →OTULFI →fda approvals ↗
    ›Aug 14, 2025approval371d agoLAZCLUZE (LAZERTINIB MESYLATE) — FDA approvallazertinib mesylate

    Sponsor: JANSSEN BIOTECH. Form: TABLET. Route: ORAL

    full page →lazertinib mesylate →fda approvals ↗
    ›Aug 14, 2025approval371d agoRYBREVANT (AMIVANTAMAB-VMJW) — FDA approvalamivantamab

    Sponsor: JANSSEN BIOTECH. Form: INJECTABLE. Route: INJECTION

    full page →amivantamab →fda approvals ↗
    ›Aug 14, 2025device pma371d agoBoston Scientific Corp — Blazer™ Open-Irrigated Ablation Catheter (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 ↗
    ›Aug 14, 2025device pma371d agoMicro Therapeutics, Inc. d/b/a ev3 Neurovascular — Pipeline™ Vantage Embolization Device with Shield Technology™ (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoAllergan — Juvéderm Voluma XC, Juvéderm Vollure XC, Juvéderm Volbella XC, Juvéderm Volux XC and SKINVIVE by Juvéderm (hereafter ref (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LMH. Advisory committee: SU. Decision: OK30

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoBoston Scientific Corp — ROTABLATOR™ Rotational Atherectomy System (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoGeneoscopy, Inc. — ColoSense® (PMA supplement)

    Supplement type: 30-Day Notice. Product code: SBB. Advisory committee: PA. Decision: OK30

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoEndotronix, Inc. — Cordella Pulmonary Artery Sensor System (CorPASS) (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoFarapulse, Inc. — FARAPULSE™ Pulsed Field Ablation System (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoBoston Scientific — Blazer™ II XP Cardiac Ablation Catheter and Cable (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 ↗
    ›Aug 14, 2025device pma371d agoAllergan — Juvéderm Ultra XC, and Juvéderm Ultra Plus XC (hereafter referred to as Ultra XC and Ultra Plus XC) (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LMH. Advisory committee: SU. Decision: OK30

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoSiemens Medical Solutions Diagnostics Limited — IMMULITE 2000 Systems Free Prostate-Specific Antigen (Free PSA) (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MTG. Advisory committee: IM. Decision: OK30

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoSiemens Healthcare Diagnostics, Inc. — IMMULITE 2000 Prostate-Specific Antigen (PSA) (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MTF. Advisory committee: IM. Decision: OK30

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoColoplast Corp. — Titan Inflatable Penile Prosthesis (PMA supplement)

    Supplement type: Real-Time Process. Product code: FHW. Advisory committee: GU. Decision: APPR

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoMedtronic, Inc. — Medtronic CoreValve™ Evolut™ PRO Transcatheter Aortic Valve; Medtronic Evolut™ PRO+ Transcatheter Aortic Valve; Medtroni (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoBoston Scientific Corp — Blazer™ II Cardiac Ablation System and Cable (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoBoston Scientific Corporation — POLARx™ Cryoablation System (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoMedtronic Neuromodulation — Master Restore™, Itrel™, Synergy™, Intellis™, Vanta™ and Inceptiv™ Spinal Cord Stimulation Systems and Pisces™, Specify™ (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma371d agoIntegrum AB — OPRA™ Implant System (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 14, 2025device 510k371d agoGuangzhou Ajax Medical Equipment Co., Ltd. — Cassette Autoclave (ACA5) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k371d agoShenzhen Kaiyan Medical Equipment Co., Ltd. — TRUDERMAL Pro (ZLD-390) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k371d agoGM Dos Reis Industria e Comercio Ltda. — Stitch Cerclage – Suture Tapes (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k371d agoForus Health Pvt.Ltd — 3nethra neo HD FA; 3nethra neo HD (510k cleared)

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

    full page →fda device 510k ↗
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