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8,833 catalysts · 3,230 8k filing · 1,702 grant · 1,000 device adverse event · 795 approval · 621 device 510k · 584 earnings

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  • 8k filing3,230
  • grant1,702
  • device adverse event1,000
  • approval795
  • device 510k621
  • earnings584
device pma
467
  • device recall191
  • phase 2 completion172
  • recall162
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Feb 23, 2026

    50
    ›Feb 24, 2026device pma171d agoBoston Scientific Corporation — Axonics Sacral Neuromodulation System (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: QON. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Feb 24, 2026device pma171d agoABBOTT MEDICAL — Amplatzer™ Amulet™ Left Atrial Appendage Occluder (Amulet) (PMA supplement)

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

    full page →fda device pma ↗
    ›Feb 24, 2026grant171d agoWASHINGTON UNIVERSITY — Dissecting the Impact of HIV-Induced Immunometabolic Perturbation on Tubercul...

    AI grant. $427,623. PI: George Kyei

    full page →nih reporter ↗
    ›Feb 24, 2026grant171d agoUNIVERSITY OF CONNECTICUT STORRS — Role of Alternate Ribosome Binding in Pathogenesis

    AI grant. $447,604. PI: VICTORIA L ROBINSON

    full page →nih reporter ↗
    ›Feb 24, 2026grant171d agoUNIVERSITY OF VIRGINIA — Pathogenesis of the concentric hypertrophy of the kidney arteriolesUniversity of Virginia

    DK grant. $797,878. PI: ROBERTO Ariel GOMEZ

    full page →nih reporter ↗
    ›Feb 24, 2026grant171d agoUNIVERSITY OF CALIFORNIA SANTA CRUZ — The multifaceted pathways of astrovirus entry and egress

    GM grant. $422,677. PI: Valerie Cortez

    full page →nih reporter ↗
    ›Feb 24, 2026grant171d agoUNIVERSITY OF PITTSBURGH AT PITTSBURGH — Technology knowledge optimization for type 1 diabetes in schools (TeKnO T1D: ...

    NR grant. $472,950. PI: Christine March

    full page →nih reporter ↗
    ›Feb 24, 2026grant171d agoUNIVERSITY OF OREGON — Molecular Mechanisms of Antimicrobial Resistance from Machine Learning Augmen...

    GM grant. $401,285. PI: Dhiman Ray

    full page →nih reporter ↗
    ›Feb 24, 2026grant171d agoUNIVERSITY OF ROCHESTER — Influence of pregnancy and the gut microbiome on methylmercury metabolism and...University of Rochester

    ES grant. $415,613. PI: MATTHEW D RAND

    full page →nih reporter ↗
    ›Feb 24, 2026grant171d agoMAYO CLINIC ROCHESTER — Regulation of target cell survival by TBK1 and IKKeMayo Clinic

    AI grant. $624,521. PI: ADRIAN T TING

    full page →nih reporter ↗
    ›Feb 24, 2026grant171d agoUNIVERSITY OF CALIFORNIA, SAN DIEGO — Camptothecin analogs as "block and lock" agents for HIVUniversity of California San Diego

    AI grant. $718,637. PI: Nadejda S Beliakova-Bethell

    full page →nih reporter ↗
    ›Feb 25, 2026approval170d agoWEGOVY (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Feb 25, 2026approval170d agoWEGOVY (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Feb 25, 2026approval170d agoSAXENDA (LIRAGLUTIDE) — FDA approvalNovo Nordisk Inc

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Feb 25, 2026approval170d agoZIOPTAN (TAFLUPROST) — FDA approvaltafluprost

    Sponsor: THEA PHARMA. Form: SOLUTION/DROPS. Route: OPHTHALMIC

    full page →tafluprost →fda approvals ↗
    ›Feb 25, 2026approval170d agoZEPBOUND (TIRZEPATIDE) — FDA approvalZEPBOUND

    Sponsor: ELI LILLY AND CO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →ZEPBOUND →fda approvals ↗
    ›Feb 25, 2026approval170d agoENTYVIO (VEDOLIZUMAB) — FDA approvalTakeda Pharmaceuticals USA Inc

    Sponsor: TAKEDA PHARMS USA. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Feb 25, 2026approval170d agoDEXMEDETOMIDINE HYDROCHLORIDE — FDA approvalBioXcel Therapeutics, Inc.

    Sponsor: DR REDDYS. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Feb 25, 2026approval170d agoHYDROCORTISONE — FDA approvalET-800

    Sponsor: APPCO. Form: TABLET. Route: ORAL

    full page →ET-800 →fda approvals ↗
    ›Feb 25, 2026approval170d agoCETIRIZINE HYDROCHLORIDE — FDA approvalCETIRIZINE HYDROCHLORIDE

    Sponsor: RUBICON RESEARCH. Form: SOLUTION. Route: ORAL

    full page →CETIRIZINE HYDROCHLORIDE →fda approvals ↗
    ›Feb 25, 2026approval170d agoBUPROPION HYDROCHLORIDE — FDA approvalSenores Pharmaceuticals Inc

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

    full page →fda approvals ↗
    ›Feb 25, 2026approval170d agoONDANSETRON HYDROCHLORIDE — FDA approvalondansetron hydrochloride CR

    Sponsor: DR REDDYS LABS LTD. Form: TABLET. Route: ORAL

    full page →ondansetron hydrochloride CR →fda approvals ↗
    ›Feb 25, 2026approval170d agoEVEROLIMUS — FDA approvalPostsurgical Therapeutics Inc

    Sponsor: EUGIA PHARMA. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Feb 25, 2026approval170d agoANASTROZOLE — FDA approvalStason Pharmaceuticals Inc

    Sponsor: BEIJING YILING. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Feb 25, 2026approval170d agoONDANSETRON HYDROCHLORIDE — FDA approvalondansetron hydrochloride CR

    Sponsor: RISING. Form: TABLET. Route: ORAL

    full page →ondansetron hydrochloride CR →fda approvals ↗
    ›Feb 25, 2026approval170d agoENTYVIO (VEDOLIZUMAB) — FDA approvalTakeda Pharmaceuticals USA Inc

    Sponsor: TAKEDA PHARMS USA. Form: INJECTABLE. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Feb 25, 2026approval170d agoJUXTAPID (LOMITAPIDE MESYLATE) — FDA approvalChiesi USA Inc

    Sponsor: CHIESI. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Feb 25, 2026approval170d agoDESMODA (DESMOPRESSIN ACETATE) — FDA approvaldesmopressin acetate

    Sponsor: ETON. Form: SOLUTION. Route: ORAL

    full page →desmopressin acetate →fda approvals ↗
    ›Feb 25, 2026approval170d agoLAMOTRIGINE — FDA approvalLAMOTRIGINE

    Sponsor: ALEMBIC. Form: TABLET, ORALLY DISINTEGRATING. Route: ORAL

    full page →LAMOTRIGINE →fda approvals ↗
    ›Feb 25, 2026device 510k170d agoBecton, Dickinson and Company (BD) — BD Surgiphor™ Antimicrobial Irrigation System (910110) (510k cleared)BECTON DICKINSON & CO

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

    full page →fda device 510k ↗
    ›Feb 25, 2026device 510k170d agoSpinal Elements, Inc. — Ventana™ A Anterior Lumbar Interbody System (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 25, 2026device 510k170d agoZhejiang Yikang Medical Technology Co., Ltd. — Electric wheelchair (510k cleared)Zhejiang Xinkanghe Biomedical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›Feb 25, 2026device 510k170d agoMedline Industries, LP — Konig Bell Circumcision Clamp (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 25, 2026device 510k170d agoGrindguard, Inc. — Remi Impression Material (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 25, 2026device 510k170d agoMako Surgical Corp. — Mako Total Knee Application (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 25, 2026device 510k170d agoMighty Oak Medical — FIREFLY® Pedicle Screw Navigation Guide (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 25, 2026device pma170d agoNovocure, GmbH — Optune Gio® (PMA supplement)NovoCure Ltd

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

    full page →fda device pma ↗
    ›Feb 25, 2026device pma170d agoBoston Scientific Corporation — Axonics Sacral Neuromodulation System (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: EZW. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Feb 25, 2026device pma170d agoBoston Scientific Corporation — Axonics Sacral Neuromodulation System (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: QON. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Feb 25, 2026device pma170d agoABBOTT MEDICAL — TriClip™ G5 Delivery System (TCDS0801-NT, TCDS0801-NTW, TCDS0801-XT, TCDS0801-XTW) (PMA supplement)

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

    full page →fda device pma ↗
    ›Feb 25, 2026device pma170d agoIntegra Lifesciences Corp. — INTEGRA ® Dermal Regeneration Template; Integra® Meshed Dermal Regeneration Template; Integra® Omnigraft Dermal Regenera (PMA supplement)INTEGRA LIFESCIENCES HOLDINGS CORP

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

    full page →fda device pma ↗
    ›Feb 25, 2026device pma170d agoABBOTT MEDICAL — MitraClip™ G5 Delivery System (CDS0801-NT, CDS0801-NTW, CDS0801-XT, CDS0801-XTW) (PMA supplement)

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

    full page →fda device pma ↗
    ›Feb 25, 2026device pma170d agoNovocure, GmbH — Optune Lua® (PMA supplement)NovoCure Ltd

    Supplement type: 30-Day Notice. Product code: SDA. Advisory committee: AN. Decision: OK30

    full page →fda device pma ↗
    ›Feb 25, 2026device pma170d agoBoston Scientific Corp — AMS 800™ Artificial Urinary Sphincter (AUS) (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: EZY. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Feb 25, 2026device recall170d agoSynthes (USA) Products LLC device recall (Cls II)

    2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US. — Reason: A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall170d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 3005PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the PKS electrical generator. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall170d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus PKS Cutting Forceps w/Cord, 5mm 24cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920000PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the PKS electrical generator. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall170d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Product Description: An assembly of devices intended to generate and apply radio-frequency (RF) alternating current to soft tissues for cutting and coagulation during an endoscopic or open surgical procedure. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall170d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus Everest Bipolar Cutting Forceps, 5 mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3005 Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the bipolar outputs of compatible generators. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall170d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3006 Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the bipolar outputs of compatible generators. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
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