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13,283 catalysts · 3,603 8k filing · 2,377 grant · 2,049 approval · 1,383 device 510k · 1,000 device adverse event · 930 device pma

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  • 8k filing3,603
  • grant2,377
  • approval2,049
  • device 510k1,383
  • device adverse event1,000
  • device pma930
device recall
912
  • earnings585
  • recall364
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Nov 17, 2025

    50
    ›Nov 20, 2025device recall283d agoCareFusion 303, Inc. device recall (Cls II)

    BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower, REF: 352, BD Pyxis Pro 7-Drawer Auxiliary, REF: 1149-00, BD Pyxis Pro 7- Drawer Auxiliary with Secure Tower, REF: 1152-00, BD Pyxis Pro MedStation Main, REF: 1155-00, BD Pyxis CII Safe ES, REF: 1116-00 — Reason: Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a duplicate address, which causes an error and the drawer to fail, which may lead to inability or delay in accessing stored items, delay in the replenishment of ADCs or patient specific medications stored outside of ADCs. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 20, 2025device recall283d agoMedtronic Neuromodulation device recall (Cls II)

    Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT900A CLINICIAN TABLET US CT900B PROG CT900B CLINICIAN TABLET EU -UK CT900C PROG CT900C CLINICIAN TABLET UK CT900D PROG CT900D CLINICIAN TABLET GLOBAL CT900E PROG CT900E CLINICIAN TABLET GLBL SMSNG CT900F PROG CT900F CLINICIAN TABLET GLBL SMSNG — Reason: Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume therapy, and the patient experienced a recurrence of underlying pain symptoms. Resolution would require surgical replacement of the INS. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 21, 2025approval282d agoKEYTRUDA (PEMBROLIZUMAB) — FDA approvalpembrolizumab

    Sponsor: MERCK SHARP DOHME. Form: SOLUTION. Route: INTRAVENOUS

    full page →pembrolizumab →fda approvals ↗
    ›Nov 21, 2025approval282d agoKEYTRUDA QLEX (PEMBROLIZUMAB) — FDA approval(berahyaluronidase alfa + pembrolizumab)

    Sponsor: MERCK SHARP DOHME. Form: INJECTABLE. Route: INJECTION

    full page →(berahyaluronidase alfa + pembrolizumab) →fda approvals ↗
    ›Nov 21, 2025approval282d agoWEGOVY (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Nov 21, 2025approval282d agoNARCAN (NALOXONE HYDROCHLORIDE) — FDA approvalEmergent Devices Inc

    Sponsor: EMERGENT. Form: SPRAY, METERED. Route: NASAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval282d agoNEXLETOL (BEMPEDOIC ACID) — FDA approvalbempedoic acid

    Sponsor: ESPERION THERAPS INC. Form: TABLET. Route: ORAL

    full page →bempedoic acid →fda approvals ↗
    ›Nov 21, 2025approval282d agoNEXLIZET (BEMPEDOIC ACID) — FDA approval(bempedoic acid + ezetimibe)

    Sponsor: ESPERION THERAPS INC. Form: TABLET. Route: ORAL

    full page →(bempedoic acid + ezetimibe) →fda approvals ↗
    ›Nov 21, 2025approval282d agoLIVTENCITY (MARIBAVIR) — FDA approvalTakeda Pharmaceuticals USA Inc

    Sponsor: TAKEDA PHARMS USA. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval282d agoURSODIOL — FDA approvalURSODIOL

    Sponsor: STRIDES PHARMA. Form: CAPSULE. Route: ORAL

    full page →URSODIOL →fda approvals ↗
    ›Nov 21, 2025approval282d agoUNLOXCYT (COSIBELIMAB-IPDL) — FDA approvalcosibelimab

    Sponsor: CHECKPOINT THERAPEUTICS INC. Form: INJECTABLE. Route: INJECTION

    full page →cosibelimab →fda approvals ↗
    ›Nov 21, 2025approval282d agoDALFAMPRIDINE — FDA approvalSolaxa Inc

    Sponsor: ALKEM LABS LTD. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval282d agoFULVESTRANT — FDA approvalFULVESTRANT

    Sponsor: AVYXA HOLDINGS. Form: SOLUTION. Route: INTRAMUSCULAR

    full page →FULVESTRANT →fda approvals ↗
    ›Nov 21, 2025approval282d agoBACLOFEN — FDA approvalBACLOFEN

    Sponsor: AUROBINDO PHARMA LTD. Form: TABLET. Route: ORAL

    full page →BACLOFEN →fda approvals ↗
    ›Nov 21, 2025approval282d agoPYLERA (BISMUTH SUBCITRATE POTASSIUM) — FDA approval

    Sponsor: LABS JUVISE. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval282d agoAKTEN (LIDOCAINE HYDROCHLORIDE) — FDA approvalLaryng-O-Jet

    Sponsor: THEA PHARMA. Form: GEL. Route: OPHTHALMIC

    full page →Laryng-O-Jet →fda approvals ↗
    ›Nov 21, 2025approval282d agoDEFLAZACORT — FDA approvalAmneal Pharmaceuticals, Inc.

    Sponsor: UPSHER SMITH LABS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval282d agoLEVETIRACETAM — FDA approvalAprecia Pharmaceuticals LLC

    Sponsor: ANDA REPOSITORY. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval282d agoPADCEV (ENFORTUMAB VEDOTIN-EJFV) — FDA approvalenfortumab vedotin

    Sponsor: ASTELLAS. Form: INJECTABLE. Route: INJECTION

    full page →enfortumab vedotin →fda approvals ↗
    ›Nov 21, 2025approval282d agoDIPRIVAN (PROPOFOL) — FDA approvalPROPOFOL

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

    full page →PROPOFOL →fda approvals ↗
    ›Nov 21, 2025approval282d agoALBUTEROL SULFATE — FDA approvalALBUTEROL SULFATE

    Sponsor: CIPLA. Form: AEROSOL, METERED. Route: INHALATION

    full page →ALBUTEROL SULFATE →fda approvals ↗
    ›Nov 21, 2025approval282d agoQOLIANA (BRIMONIDINE TARTRATE) — FDA approvalLumify

    Sponsor: SANDOZ. Form: SOLUTION/DROPS. Route: OPHTHALMIC

    full page →Lumify →fda approvals ↗
    ›Nov 21, 2025device 510k282d agoEffortmed, LLC — EffortMed PEEK Cages & Corpectomy Cages (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoNGMedical GmbH — BEE HA (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoNeuro Event Labs OY — Nelli (Version 7.11) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoDeroyal Industries, Inc. — Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory (510k cleared)ABM INDUSTRIES INC /DE/

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoFoshan Kycare Medical Equipment Co., Ltd. — Oxygen Concentrator (J5A) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoGraphy, Inc. — TERA HARZ Hard Denture (THD-C-500); TERA HARZ Hard Denture (THD-C-1000); TERA HARZ Hard Denture (THD-LP-500); TERA HARZ Hard Denture (THD-LP-1000); TERA HARZ Hard Denture (THD-P-500); TERA HARZ Hard Denture (THD-P-1000); TERA HARZ Hard Denture (THD-CP-500); TERA HARZ Hard Denture (THD-CP-1000) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoCentrix, Inc. — FluoroDose Varnish (510k cleared)CentricsBio Inc

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoJoint Preservation Innovations, LLC — Articulator Arthroscopic Bur (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoEveryway Medical Instruments Co.,Ltd — Li-Battery Powered OTC TENS/EMS Combination Stimulator, Model Z4 (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoStaclear, Inc. — StaClear Syringe (SC250AN); StaClear Syringe (SC250LS); StaClear Syringe (SC250LL) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoTerumo Corporation — Pen Injector Needle 32.5 (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoPhasor Health, LLC — LEGACY (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoSuzhou Master Machinery Manufacturing Co.,Ltd — Manual Wheelchair (HM305-Air1, HM305-Air2) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoIcardio.Ai — CardioVision (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoArchy Dental, Inc. — Archy Dental Imaging (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoIntradin (Shanghai) Machinery Co., Ltd. — Powered Mobility Scooter (PMS105, GUT177, GCAT047) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoCeribell, Inc. — Ceribell Infant Seizure Detection Software (510k cleared)Ceribell, Inc.

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k282d agoDentsply Sirona — Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants (510k cleared)DENTSPLY SIRONA Inc.

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device pma282d agoLife Technologies Corporation — Oncomine™ Dx Target Test (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: PQP. Advisory committee: PA. Decision: APPR

    full page →fda device pma ↗
    ›Nov 21, 2025device pma282d agoTherakos Development Limited — THERAKOS® CELLEX® Photopheresis System (CELLEX), THERAKOS® CELLEX® Photopheresis Procedural Kit (CLXUSA and CLXECP), THE (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 21, 2025device pma282d agoGE Healthcare — Senographe Pristina 3D (PMA supplement)HCA Healthcare, Inc.

    Supplement type: Normal 180 Day Track. Product code: OTE. Advisory committee: RA. Decision: APPR

    full page →fda device pma ↗
    ›Nov 21, 2025device pma282d agoQiagen — QuantiFERON-TB Gold Plus Test (PMA supplement)QIAGEN N.V.

    Supplement type: Real-Time Process. Product code: NCD. Advisory committee: MI. Decision: APPR

    full page →fda device pma ↗
    ›Nov 21, 2025device pma282d agoPhysio-Control, Inc. — LIFEPAK® 35 monitor/defibrillator (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 21, 2025device recall282d agoMedline Industries, LP device recall (Cls II)

    Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK,OXYGEN,UND CHIN,MED CO OUS ONLY; HUD1035 O2 MASK,MED CONC,SHORT,PEDI,7' TUB SC; HUD1042 O2 MASK,MED CONC,PEDI,7' TUB SC; HUD1930 O2 MASK,MED CONC,ADULT,7' TUB UC; HUDRHO41U MASK,OXYGEN,MEDIUM-CONCENTRATION,7,SC — Reason: Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and patient may experience shortness of breath leading to hypoxia, which may require medical intervention to prevent further respiratory deterioration. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 21, 2025device recall282d agoFresenius Kabi USA, LLC device recall (Cls II)Fresenius Kabi USA LLC

    Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005. — Reason: Emphasizing instructions for LVP duration programming located in the IFU. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 21, 2025device recall282d agoRoche Diagnostics Operations, Inc. device recall (Cls II)

    The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with streptavidin-coated microparticles and electrochemiluminescence detection. Patient serum sample is incubated with pretreatment reagent PT1 and the reconstituted PT2 containing a pre-formed immunocomplex of solubilized porcine TSH receptor (pTSHR) and biotinylated anti-pTSHR mouse monoclonal antibody. — Reason: Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as delay of treatment or incorrect treatment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 22, 2025device 510k281d agoKarl Storz SE & CO. KG — KARL STORZ Cholangiography Set (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 22, 2025device pma281d agoMedtronic, Inc. — Medtronic DBS Therapy for Dystonia (PMA supplement)Medtronic plc

    Supplement type: Panel Track. Product code: SGS. Advisory committee: NE. Decision: APPR

    full page →fda device pma ↗
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