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calendar

15,048 catalysts · 3,603 8k filing · 2,723 grant · 2,426 approval · 1,714 device 510k · 1,264 device recall · 1,172 device pma

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  • 8k filing3,603
  • grant2,723
  • approval2,426
  • device 510k1,714
  • device recall1,264
  • device pma1,172
device adverse event
1,000
  • earnings585
  • recall481
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Oct 20, 2025

    50
    ›Oct 22, 2025recall311d agoEndo USA, Inc. recall (Cls III)Par Pharmaceutical Inc

    Everolimus tablets 5mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977, NDC 49884-125-91 — Reason: Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C. — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025recall311d agoSV Labs Prescott Corporation recall (Cls II)

    Aloe Up Sport Performance Sunscreen Lotion SPF 30, 1 FL OZ (30 mL) per tube, Mfd. for: ALOE UP, 9700 W. 76th St., Ste 112, Eden Prairie, Minnesota 55344 — Reason: cGMP deviations: the firm released and distributed product which failed total aerobic microbial count testing. — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 22, 2025device 510k311d agoProsidyan, Inc. — FIBERGRAFT™ BG Putty GPS Bone Graft Substitute FIBERGRAFT™ BG Putty Bone Graft Substitute FIBERGRAFT™ AERIDYAN™ Matrix Bone Graft Substitute FIBERGRAFT™ BG Matrix Bone Graft Substitute (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoYorlabs, Inc. — XC11 ICE System, USA (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoZeus Scientific — Alegria Flash CTD Screen (510k cleared)Dawn Sea Therapeutics

    Product code: LLL. Advisory committee: Immunology. Type: Traditional

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoImeka Solutions, Inc. — ANDI 2.0 (510k cleared)UL Solutions Inc.

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoQIAGEN GmbH — QIAstat-Dx Gastrointestinal Panel 2; QIAstat-Dx GI Panel 2 Mini B&V; QIAstat-Dx GI Panel 2 Mini B (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoGenesys Spine — SIros-X System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoCosmo Far East Technology Limited — Hair Growth Laser Cap (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoDatex-Ohmeda, Inc. — Giraffe OmniBed Carestation (CS1); Giraffe Incubator Carestation (CS1) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoDcstar, Inc. — Mandibular Advancement Device L07 (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoRti Surgical, Inc. — Pre-Sutured Tendon (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoACON Laboratories, Inc. — Flowflex Plus RSV + Flu A/B + COVID Home Test (510k cleared)Alcon Laboratories Inc

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoSirona Medical — Sirona Advanced Imaging Suite (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoNingbo Youhe Electrical Appliance Technology Co., Ltd. — electric breast pump (FZ-P8); electric breast pump (YH-P8); electric breast pump (YH-P8X) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoIntervene — Recana Thrombectomy Catheter System (FG014. FG015, FG016, FG017, FG018, FG019, FG020) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoMaxx Orthopedics, Inc. — Freedom® Total Knee System – Titan PCK Components (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoBalt USA, LLC — Carrier XL Delivery Catheter (510k cleared)Bayer USA LLC

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

    full page →fda device 510k ↗
    ›Oct 22, 2025device 510k311d agoGuangzhou Wondfo Biotech Co., Ltd. — WELLlife COVID-19 Antigen Test Rx (510k cleared)

    Product code: QVF. Advisory committee: Microbiology. Type: Dual Track

    full page →fda device 510k ↗
    ›Oct 22, 2025device pma311d agoAbbott Vascular — RX Herculink Elite (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoBoston Scientific Corp — G124 MOMENTUM™ CRT-D, G125 MOMENTUM™ CRT-D, G126 MOMENTUM™ CRT-D, G128 MOMENTUM, G138 MOMENTUM™ X4 CRT-D, G140 INOGEN™ C (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoGuidant Corp. — U125 VALITUDE™ CRT-P,U128 VALITUDE™ X4 CRT-P,U225 VISIONIST™ CRT-P,U226 VISIONIST™ CRT-P,U228 VISIONIST™ X4 CRT-P (PMA supplement)Guident Corp.

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoAbbott Vascular — RX Acculink (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoLife Technologies Corporation — Oncomine Dx Express Test (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoTransMedics, Inc. — Organ Care System™ (OCS™) Heart System (PMA supplement)TransMedics Group, Inc.

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoABBOTT MEDICAL — Esprit BTK RX System; Esprit BTK OTW System (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoBoston Scientific Corp — L100 ESSENTIO™ SR,L101 ESSENTIO™ DR,L121 ESSENTIO™ EL DR,L200 PROPONENT™ SR,L201 PROPONENT™ DR,L221 PROPONENT™ EL DR,L30 (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoAbbott Vascular — XIENCE Alpine™ Everolimus Eluting Coronary Stent System (XIENCE Alpine OTW) (PMA supplement)Postsurgical Therapeutics Inc

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoMedtronic, Inc. — Medtronic Evolut™ PRO+ Delivery Catheter System (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoBoston Scientific — L110 ESSENTIO™ MRI SR,L111 ESSENTIO™ MRI DR,L131 ESSENTIO™ MRI EL DR,L210 PROPONENT,L211 PROPONENT,L231 PROPONENT,L310 A (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoLimFlow, Inc. — LimFlow System (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoCook Ireland, Ltd. — Zilver Flex® 35 Vascular Stent (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: NIO. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d 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 ↗
    ›Oct 22, 2025device pma311d agoAbbott Vascular, Inc. — Absolute Pro Vascular (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoOn-X Life Technologies, Inc. — On-X Prosthetic Heart Valves and Ascending Aortic Prothesis (AAP) (PMA supplement)Lifeloc Technologies, Inc

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoTransMedics, Inc. — Organ Care System™ (OCS™) Lung System (PMA supplement)TransMedics Group, Inc.

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoBoston Scientific — D010 INOGEN™ MINI ICD VR, D011 INOGEN™ MINI ICD VR, D012 INOGEN™ MINI ICD DR, D013 INOGEN™ MINI ICD DR, D020 DYNAGEN™ MI (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoOn-X Life Technologies, Inc. — On-X Prosthetic Heart Valves and Ascending Aortic Prothesis (PMA supplement)Lifeloc Technologies, Inc

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoTransMedics, Inc. — Organ Care System™ (OCS™) Liver (PMA supplement)TransMedics Group, Inc.

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoBoston Scientific Corporation — A209 SICD Gen 2,A219 SICD MRI (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoInspire Medical Systems — Inspire® Upper Airway Stimulation (PMA supplement)Inspire Medical Systems, Inc.

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoBoston Scientific — D010 INOGEN™ MINI ICD VR,D011 INOGEN™ MINI ICD VR,D012 INOGEN™ MINI ICD DR,D013 INOGEN™ MINI ICD DR,D020 DYNAGEN™ MINI I (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoQIAGEN GmbH — therascreen® PIK3CA RGQ PCR Kit (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: OWD. Advisory committee: MG. Decision: APPR

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoBoston Scientific Corp — G124 MOMENTUM™ CRT-D,G125 MOMENTUM™ CRT-D,G126 MOMENTUM™ CRT-D,G128 MOMENTUM,G138 MOMENTUM™ X4 CRT-D,G140 INOGEN™ CRT-D, (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoOn-X Life Technologies, Inc. — On-X Prosthetic Heart Valves; On-X Ascending Aortic Prothesis (PMA supplement)Lifeloc Technologies, Inc

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

    full page →fda device pma ↗
    ›Oct 22, 2025device pma311d agoOn-X Life Technologies, Inc. — On-X Heart Valve; On-X Ascending Aortic Prosthesis (PMA supplement)Lifeloc Technologies, Inc

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

    full page →fda device pma ↗
    ›Oct 22, 2025device recall311d agoOlympus Corporation of the Americas device recall (Cls II)

    Olympus Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S — Reason: Firm is initiating a removal due to continued reports of adverse events. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 22, 2025device recall311d agoOlympus Corporation of the Americas device recall (Cls II)

    Olympus Thunderbeat, 5mm, 35 cm, Pistol Grip — Reason: Firm is initiating a removal due to continued reports of adverse events. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 22, 2025device recall311d agoOlympus Corporation of the Americas device recall (Cls II)

    Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip Type S — Reason: Firm is initiating a removal due to continued reports of adverse events. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 22, 2025device recall311d agoOlympus Corporation of the Americas device recall (Cls II)

    Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip — Reason: Firm is initiating a removal due to continued reports of adverse events. — Status: Ongoing

    full page →fda device recalls ↗
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