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21,449 catalysts · 4,728 grant · 3,674 8k filing · 3,562 device 510k · 2,929 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • 8k filing3,674
  • device 510k3,562
  • approval2,929
  • device pma2,000
  • device recall2,000
  • device adverse event1,000
  • recall891
  • earnings585
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Oct 20, 2025

    50
    ›Oct 24, 2025approval314d agoGLYXAMBI (EMPAGLIFLOZIN) — FDA approval(empagliflozin + linagliptin)

    Sponsor: BOEHRINGER INGELHEIM. Form: TABLET. Route: ORAL

    full page →(empagliflozin + linagliptin) →fda approvals ↗
    ›Oct 24, 2025approval314d agoLETROZOLE — FDA approvalHikma Pharmaceuticals Plc

    Sponsor: HIKMA PHARMS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 24, 2025approval314d agoANASTROZOLE — FDA approvalANASTROZOLE

    Sponsor: SANDOZ. Form: TABLET. Route: ORAL

    full page →ANASTROZOLE →fda approvals ↗
    ›Oct 24, 2025approval314d agoSYNJARDY (EMPAGLIFLOZIN) — FDA approvalSYNJARDY

    Sponsor: BOEHRINGER INGELHEIM. Form: TABLET. Route: ORAL

    full page →SYNJARDY →fda approvals ↗
    ›Oct 24, 2025approval314d agoTRIJARDY XR (EMPAGLIFLOZIN) — FDA approval(empagliflozin + linagliptin + metformin hydrochloride) ER

    Sponsor: BOEHRINGER INGELHEIM. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →(empagliflozin + linagliptin + metformin hydrochloride) ER →fda approvals ↗
    ›Oct 24, 2025approval314d agoROCURONIUM BROMIDE — FDA approvalROCURONIUM BROMIDE

    Sponsor: B BRAUN MEDICAL. Form: SOLUTION. Route: INTRAVENOUS

    full page →ROCURONIUM BROMIDE →fda approvals ↗
    ›Oct 24, 2025approval314d agoJARDIANCE (EMPAGLIFLOZIN) — FDA approvalSYNJARDY

    Sponsor: BOEHRINGER INGELHEIM. Form: TABLET. Route: ORAL

    full page →SYNJARDY →fda approvals ↗
    ›Oct 24, 2025approval314d agoNEOSTIGMINE METHYLSULFATE — FDA approvalNEOSTIGMINE METHYLSULFATE

    Sponsor: AMPHASTAR PHARMS INC. Form: SOLUTION. Route: INTRAVENOUS

    full page →NEOSTIGMINE METHYLSULFATE →fda approvals ↗
    ›Oct 24, 2025approval314d agoRIVAROXABAN — FDA approvalRIVAROXABAN

    Sponsor: MSN. Form: TABLET. Route: ORAL

    full page →RIVAROXABAN →fda approvals ↗
    ›Oct 24, 2025approval314d agoANASTROZOLE — FDA approvalANASTROZOLE

    Sponsor: HIKMA. Form: TABLET. Route: ORAL

    full page →ANASTROZOLE →fda approvals ↗
    ›Oct 24, 2025device 510k314d agoCoroventis Research AB — CoroFlow Cardiovascular System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoBeijing Fule Science & Technology Development Co., Ltd. — Fule Spinal Fixation System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoMedtronic Sofamor Danek USA, Inc. — CD Horizon™ Spinal System (510k cleared)Medtronic USA Inc

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoPhilips Medical Systems Nederland B.V. — LumiGuide Equipment R2.1; LumiGuide Wire; LumiGuide 3D Hub (510k cleared)

    Product code: DQK. Advisory committee: Cardiovascular. Type: Abbreviated

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoVesalio, Inc. — Vesalio Peripheral System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoOlympus Medical Systems Corp. — Single-Use Fine Needle Biopsy (FNB) device (NA-U210H) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoDexcowin Global, Inc. — Cocoon Solo (DX-7020s) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoMedivance, Inc. — Arctic Sun Temperature Management System (Model 5000) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoHowmedica Osteonics Corp., Dba Stryker Orthopaedics — Triathlon® Total Knee System - Triathlon® Gold Femoral Components (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoAbbott Ireland — Glucose2 (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoPhilips Medical Systems B.V. — Azurion R3.1 (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoSpectrum Spine, Inc. — Expandable Titanium PLIF/TLIF System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoMedline Industries, LP — Medline Bag Decanter (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoWandercraft SAS — Atalante X (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoMedtronic - Sofradim Production — Parietene™ Flat Sheet Mesh (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoSiemens Healthineers AG — Syngo Carbon Clinicals (VA41) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoJkh Health Co., Ltd. — Cryon-X Cold Compression (510k cleared)

    Product code: IRP. Advisory committee: Physical Medicine. Type: Special

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoSolutions For Tomorrow AB — Mobile X-ray unit (!M1) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoGood Sleep CO Pte , Ltd. — Hushd Pro Z-Link (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoAngioDynamics, Inc. — AngioVac Cannula (510k cleared)ANGIODYNAMICS INC

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoRoche Diagnostics — CoaguChek XS Plus System (510k cleared)

    Product code: GJS. Advisory committee: Hematology. Type: Special

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoMedtronic Sofamor Danek USA, Inc. — Infinity™ OCT System (510k cleared)Medtronic USA Inc

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoUnity Medical, Inc. — VersaD Delivery Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device 510k314d agoManteia Technologies Co., Ltd. — AccuCheck (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 24, 2025device pma314d agoBoston Scientific Corp — ACUITY X4 Leads (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoBausch & Lomb, Inc. — Bausch & Lomb SofLens® (polymacon) Contact Lenses (PMA supplement)Bausch & Lomb Corp

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

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoJohnson & Johnson Surgical Vision, Inc. — TECNIS Symfony Toric II OptiBlue Extended Range of Vision IOL with TECNIS Simplicity Delivery System, Models DXW150-375; (PMA supplement)JOHNSON & JOHNSON

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

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoGeneoscopy, Inc. — ColoSense® (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoBiotronik, Inc. — Edora 8 HF-T QP; Edora 8 HF-T; Evity 8 HF-T QP; Evity 8 HF-T; Enitra 8 HF-T QP; Enitra 8 HF-T; Enticos 8 HF-T QP; Entico (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: NKE. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoBoston Scientific — ENDOTAK RELIANCE Leads (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoBiotronik, Inc. — Acticor 7 VR-T; Rivacor 7 VR-T; Rivacor 5 VR-T; Rivacor 3 VR-T; Acticor 7 VR-T DX; Rivacor 7 VR-T DX; Rivacor 5 VR-T DX; (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: MRM. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoBoston Scientific — FINELINE II Leads (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoBoston Scientific Corp — Eluvia™ Drug-Eluting Vascular Stent System (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoBoston Scientific Corporation — AGENT™ Paclitaxel-Coated Balloon Catheter (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoBoston Scientific Corporation — Innova™ Vascular Self-Expanding Stent System (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoBiotronik, Inc. — Edora 8 DR-T; Evity 8 DR-T; Enitra 8 DR-T; Enticos 8 DR-T; Evity 6 DR-T; Enitra 6 DR-T; Edora 8 DR; Enitra 6 DR; Edora 8 (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: DXY. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoMerz North America, Inc. — Belotero Balance (+) Lidocaine Dermal Filler (PMA supplement)Sustained Therapeutics Inc

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

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoBoston Scientific Corporation — Ranger™ Paclitaxel-Coated PTA Balloon Catheter (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 24, 2025device pma314d agoTusker Medical, Inc. — Tula® System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: QJA. Advisory committee: EN. Decision: OK30

    full page →fda device pma ↗
    ›Oct 24, 2025device recall314d agoEdan Diagnostics device recall (Cls II)

    Brand Name: EDAN Product Name: Fetal Monitor Model/Catalog Number: F2, F3 Product Description: The devices are bedside fetal and maternal monitors, which are used to monitor the physiological parameters of pregnant women including the fetus from 28 weeks gestation. The devices may be used antepartum as well as during labor and delivery. Component: No — Reason: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device. — Status: Ongoing

    full page →fda device recalls ↗
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    $BSX48.08-0.46%
    $JNJ275.21+1.48%
    $AMPH23.68+3.14%
    $BSX48.08-0.46%
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    $ANGO13.82-2.81%
    $BSX48.08-0.46%
    $BSX48.08-0.46%
    $BSX48.08-0.46%
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    $BSX48.08-0.46%