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21,783 catalysts · 4,728 grant · 4,110 device 510k · 3,189 8k filing · 3,118 approval · 2,000 device pma · 2,000 device recall

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2026-08-10: 0 catalysts2026-08-11: 0 catalysts2026-08-12: 0 catalysts2026-08-13: 19 catalysts2026-08-14: 4 catalysts2026-08-15: 0 catalysts2026-08-16: 0 catalysts2026-08-17: 1 catalyst2026-08-18: 2 catalysts2026-08-19: 3 catalysts2026-08-20: 0 catalysts2026-08-21: 0 catalysts2026-08-22: 0 catalysts2026-08-23: 0 catalysts2026-08-24: 0 catalysts2026-08-25: 0 catalysts2026-08-26: 1 catalyst2026-08-27: 1 catalyst2026-08-28: 0 catalysts2026-08-29: 0 catalysts2026-08-30: 0 catalysts2026-08-31: 0 catalysts2026-09-01: 1 catalyst2026-09-02: 0 catalysts2026-09-03: 1 catalyst2026-09-04: 0 catalysts2026-09-05: 0 catalysts2026-09-06: 0 catalysts2026-09-07: 0 catalysts2026-09-08: 0 catalysts2026-09-09: 0 catalysts2026-09-10: 0 catalysts2026-09-11: 0 catalysts2026-09-12: 0 catalysts2026-09-13: 0 catalysts2026-09-14: 0 catalysts2026-09-15: 0 catalysts2026-09-16: 0 catalysts2026-09-17: 0 catalysts2026-09-18: 0 catalysts2026-09-19: 0 catalysts2026-09-20: 0 catalysts2026-09-21: 0 catalysts2026-09-22: 0 catalysts2026-09-23: 2 catalysts2026-09-24: 0 catalysts2026-09-25: 0 catalysts2026-09-26: 0 catalysts2026-09-27: 0 catalysts2026-09-28: 0 catalysts2026-09-29: 0 catalysts2026-09-30: 0 catalysts2026-10-01: 0 catalysts2026-10-02: 0 catalysts2026-10-03: 0 catalysts2026-10-04: 0 catalysts2026-10-05: 0 catalysts2026-10-06: 0 catalysts2026-10-07: 0 catalysts2026-10-08: 2 catalysts2026-10-09: 0 catalysts2026-10-10: 0 catalysts2026-10-11: 0 catalysts2026-10-12: 0 catalysts2026-10-13: 1 catalyst2026-10-14: 1 catalyst2026-10-15: 0 catalysts2026-10-16: 0 catalysts2026-10-17: 0 catalysts2026-10-18: 0 catalysts2026-10-19: 1 catalyst2026-10-20: 2 catalysts2026-10-21: 2 catalysts2026-10-22: 2 catalysts2026-10-23: 1 catalyst2026-10-24: 0 catalysts2026-10-25: 0 catalysts2026-10-26: 1 catalyst2026-10-27: 8 catalysts2026-10-28: 12 catalysts2026-10-29: 21 catalysts2026-10-30: 4 catalysts2026-10-31: 0 catalysts2026-11-01: 0 catalysts2026-11-02: 9 catalysts2026-11-03: 18 catalysts2026-11-04: 22 catalysts2026-11-05: 37 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts
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  • grant4,728
  • device 510k4,110
  • 8k filing3,189
  • approval3,118
  • device pma2,000
  • device recall2,000
device adverse event
1,000
  • recall973
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Mar 17, 2025

    17
    ›Mar 21, 2025device 510k510d agoNatural Cycles Nordic AB — Natural Cycles (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoVitromed GmbH — V-GRAD (510k cleared)

    Product code: MQL. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoVentris Medical — Porous Biologic Scaffold (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoSignos, Inc. — Signos Glucose Monitoring System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoStryker Neurovascular — Excelsior XT-27 Microcatheter, Excelsior XT-27 Flex Microcatheter, Excelsior XT-27 Pre-Shaped Microcatheter, Excelsior XT-27 Flex Pre-Shaped Microcatheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoEpitel — REMI Remote EEG Monitoring System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoGuangzhou Potent Medical Equipment Joint-Stock Co., Ltd. — EHL Probe (SCDG-AS); EHL Probe (SCDG-BS); EHL Probe (SCDG-CS) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoTenon Medical — Catamaran SI Joint Fusion System (510k cleared)Tenon Medical, Inc.

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoDentis Co., Ltd. — ChecQ (AC100) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoYukon Medical, LLC — Arisure® Closed Male Luer with Spike Adapter (YM060) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoCasebioscience, Inc. — CaseMONO™ Culture (CMON); CaseMONO™ w/HEPES (WHMO); CaseBioscience® HTF (HTFC); CaseBioscience® HTF w/HEPES (HHTF) (510k cleared)BJ Bioscience Inc

    Product code: MQL. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoGuangzhou Potent Medical Equipment Joint-Stock Co., Ltd. — Electrohydraulic Lithotriptor (TCS-B3-II) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoBoston Scientific Corporation — Navigator™ HD Ureteral Access Sheath Set 11/13 F x 28cm (M0062502210); Navigator™ HD Ureteral Access Sheath Set 11/13 F x 36cm (M0062502220); Navigator™ HD Ureteral Access Sheath Set 11/13 F x 46cm (M0062502230); Navigator™ HD Ureteral Access Sheath Set 12/14 F x 28cm (M0062502240); Navigator™ HD Ureteral Access Sheath Set 12/14 F x 36cm (M0062502250); Navigator™ HD Ureteral Access Sheath Set 12/14 F x 46cm (M0062502260); Navigator™ HD Ureteral Access Sheath Set 13/15 F x 28cm (M006 (510k cleared)BOSTON SCIENTIFIC CORP

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoGetset Surgical, SA — GoLIF! Lumbar Interbody Fusion System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoPhilips Medizin Systeme Böblingen GmbH — Philips Holter Analysis System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoStryker Instruments — Consolidated Operating Room Equipment (CORE) 2 Console (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 21, 2025device 510k510d agoBecton, Dickinson and Company — BD Vacutainer® Multiple Sample Luer Adapter (510k cleared)BECTON DICKINSON & CO

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

    full page →fda device 510k ↗

    Week of Mar 24, 2025

    33
    ›Mar 24, 2025approval507d agoSPRAVATO (ESKETAMINE HYDROCHLORIDE) — FDA approvalJanssen Therapeutics

    Sponsor: JANSSEN PHARMS. Form: SPRAY. Route: NASAL

    full page →fda approvals ↗
    ›Mar 24, 2025approval
    ← prev
    page 21 of 436
    next →
    507d ago
    ORLYNVAH (PROBENECID) — FDA approvalLannett Co Inc

    Sponsor: ITERUM THERAP. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Mar 24, 2025device 510k507d agoLuma Vision Limited — VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoAbbott Molecular, Inc. — Alinity m BKV (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoXplr , Ltd. — LMNT O2 (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoAurora Spine — AERO MIS Facet Fusion System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoStryker Instruments — Sonopet iQ Ultrasonic Aspirator System (5500-050-000) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoBright Uro, Inc. — Glean Urodynamics System Male Delivery System (GUS-1000-M); Glean Urodynamics System Female Delivery System (GUS-1000-F); Glean Urodynamics System Uroflowmeter (UFM-1000 (Uroflowmeter)) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoRestor3D, Inc. — TIDAL Fusion Cage System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoControl Medical Technology, Inc. / Dba Ventiv Scientific — VentiV 7Fr -12Fr MP Mechanical Thrombectomy System (VS7-MP60S, VS7-MP90S, VS8-MP60S, VS8-MP90S, VS8-MP100B, VS10-MP100B, VS11-MP60S, VS11-MP90S, VS12-MP100B, 7F-MP60S, 7F-MP90S, 8F-MP60S, 8F-MP100B, 10F-MP100B, 11F-MP60S, 11F-MP90S, 11P-MP60S, 11P-MP90S, 12F-MP100B, V30-ASP) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoInnovasis, Inc. — Innovasis Navigation Instruments (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoInnovasis — AxTiHA® Stand-Alone ALIF System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoPAJUNK GmbH Medizintechnologie — SonoTAP and SonoTAP II (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoTotal Joint Othopedics, Inc. — Klassic Knee System - Revision Tibial Baseplate (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 24, 2025device 510k507d agoBard Peripheral Vascular, Inc. — UltraCor™ Twirl™ Breast Tissue Marker (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 25, 2025approval506d agoBLUJEPA (GEPOTIDACIN MESYLATE) — FDA approvalgepotidacin mesylate

    Sponsor: GLAXOSMITHKLINE. Form: TABLET. Route: ORAL

    full page →gepotidacin mesylate →fda approvals ↗
    ›Mar 25, 2025approval506d agoCONEXXENCE (DENOSUMAB-BNHT) — FDA approvalCONEXXENCE

    Sponsor: FRESENIUS KABI USA LLC. Form: INJECTION

    full page →CONEXXENCE →fda approvals ↗
    ›Mar 25, 2025approval506d agoTREMFYA (GUSELKUMAB) — FDA approvalguselkumab

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

    full page →guselkumab →fda approvals ↗
    ›Mar 25, 2025device 510k506d agoBolt Medical, Inc. — Bolt Intravascular Lithotripsy (IVL) System (510k cleared)B. Braun Medical Inc

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

    full page →fda device 510k ↗
    ›Mar 25, 2025device 510k506d agoInquis Medical — Aventus Thrombectomy System (IM-2100) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 26, 2025approval505d agoLORAZEPAM — FDA approvallorazepam ER

    Sponsor: RISING. Form: TABLET. Route: ORAL

    full page →lorazepam ER →fda approvals ↗
    ›Mar 26, 2025approval505d agoLORAZEPAM — FDA approvallorazepam ER

    Sponsor: RISING. Form: TABLET. Route: ORAL

    full page →lorazepam ER →fda approvals ↗
    ›Mar 26, 2025approval505d agoLORAZEPAM — FDA approvallorazepam ER

    Sponsor: RISING. Form: TABLET. Route: ORAL

    full page →lorazepam ER →fda approvals ↗
    ›Mar 26, 2025approval505d agoSTIMUFEND (PEGFILGRASTIM-FPGK) — FDA approvalSTIMUFEND

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

    full page →STIMUFEND →fda approvals ↗
    ›Mar 26, 2025approval505d agoRINVOQ LQ (UPADACITINIB) — FDA approvalupadacitinib

    Sponsor: ABBVIE. Form: SOLUTION. Route: ORAL

    full page →upadacitinib →fda approvals ↗
    ›Mar 26, 2025approval505d agoRINVOQ (UPADACITINIB) — FDA approvalupadacitinib tartrate ER

    Sponsor: ABBVIE. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →upadacitinib tartrate ER →fda approvals ↗
    ›Mar 26, 2025approval505d agoCABOMETYX (CABOZANTINIB S-MALATE) — FDA approvalcabozantinib s-malate

    Sponsor: EXELIXIS INC. Form: TABLET. Route: ORAL

    full page →cabozantinib s-malate →fda approvals ↗
    ›Mar 26, 2025recall505d agoFruit Of The Earth, Inc. recall (Cls II)CVS HEALTH Corp

    CVS Health Concealing Acne Treatment Cream, CVS, 10% benzoyl peroxide, 1 oz (28 g), Distributed by: CVS Pharmacy, Inc — Reason: Chemical contamination: presence of benzene — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall505d agoAmgen, Inc. recall (Cls II)AMGEN INC

    Neupogen (filgrastim) For Injection, 300mcg/1 mL, 1 mL Single Dose Vials, Rx Only, For Subcutaneous or Intravenous Use Only, Sterile Solution - No Preservative, Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-530-01 (vial), NDC 55513-530-10 (box). — Reason: Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall505d agoMYLAN PHARMACEUTICALS INC recall (Cls II)MIRA PHARMACEUTICALS, INC.

    Prasugrel Tablets, USP, 5 mg, 30-count bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-5185-93 — Reason: Failed Dissolution Specifications - low dissolution results — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall505d agoFDC Limited recall (Cls II)FDC Ltd

    Ciprofloxacin Ophthalmic Solution USP, 0.3% as base, package in 5 mL bottles, Rx Only, Distributed by: Leading Pharma LLC, Fairfield, NJ. Manufactured by: FDC Limited, Maharashtra, India, NDC 69315-308-05 — 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 ↗
    ›Mar 26, 2025recall505d agoMylan Institutional, Inc. recall (Cls II)Mylan Institutional Inc

    Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per carton, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in India, NDC 51079-443-20. — Reason: Super-Potent Drug: Out of specification potency results were obtained. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 26, 2025recall505d agoSlate Run Pharmaceuticals recall (Cls II)Slate Run Pharmaceuticals LLC

    Cinacalcet Hydrochloride Tablets 60 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-008-04 — Reason: CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits. — Status: Ongoing

    full page →fda recalls ↗
    $TNON0.2832-3.11%
    $BSX51.42+0.45%
    $BDX183.58+1.20%
    $MIRA0.9767-2.33%
    $EXEL50.38-1.85%
    $AMGN416.18+0.45%
    $CVS
    $ABBV248.76-0.53%
    $ABBV248.76-0.53%