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13,489 catalysts · 3,350 8k filing · 2,401 grant · 2,136 approval · 1,479 device 510k · 1,105 device recall · 1,000 device adverse event

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  • 8k filing3,350
  • grant2,401
  • approval2,136
  • device 510k1,479
  • device recall1,105
  • device adverse event1,000
  • device pma977
  • earnings584
  • recall376
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Oct 27, 2025

    50
    ›Oct 30, 2025device 510k291d agoShenzhen Kaiyan Medical Equipment Co., Ltd. — Q-Renew LLLT Hair Growth Helmet (Q-HLMT-V1) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoDetax GmbH — Freeprint® denture flex (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoImperative Care, Inc. — Zoom System (Zoom 4S Catheter) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoCarefusion (Bd) — BD Alaris Pump Infusion Set (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoArctx Medical — Arctx Cool Catheter Set (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoHangzhou AllTest Biotech Co., Ltd. — AllTest Urinary Tract Infection Test (510k cleared)Hangzhou DAC Biotech Co Ltd

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoDiasorin Molecular, LLC — Simplexa™ COVID-19/ Flu A/B & RSV Direct (MOL4450); Simplexa™ COVID-19/ Flu A/B & RSV Positive Control Pack (MOL4460) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoTaewoong Medical Co., Ltd. — Niti-S Esophageal Stent; Esophageal TTS Stent (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoMerchsource, LLC — AIR COMPRESSION BOOTS 1018195,1018196 (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoBoston Scientific Corporation — OBSIDIO™ Conformable Embolic (M0013972101010) (510k cleared)BOSTON SCIENTIFIC CORP

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoParagon Implant Mfg., LLC — GEN5 and GEN5+ Dental Implant System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoCytrellis Biosystems, Inc. — ellacor System with Micro-Coring Technology (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoViTAA Medical Solutions, Inc. — AiORTA - Plan (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoM.I.Tech Co., Ltd. — HANAROSTENT Esophagus Upper (CCC) (510k cleared)YSX Tech Co., Ltd

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device 510k291d agoBoston Scientific Corporation — Moses™ 200 D/F/L Laser Fiber (M0068130100); Moses™ 365 D/F/L Laser Fiber (M0068130110); Moses™ 550 D/F/L Laser Fiber (M0068130120) (510k cleared)BOSTON SCIENTIFIC CORP

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

    full page →fda device 510k ↗
    ›Oct 30, 2025device pma291d agoMedtronic, Inc. — SYNERGYST II PULSE GENERATOR MODELS 7070 & 7071 (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Oct 30, 2025device pma291d agoSiemens Medical Solutions Diagnostics Limited — IMMULITE 2000 Free PSA (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MTG. Advisory committee: IM. Decision: OK30

    full page →fda device pma ↗
    ›Oct 30, 2025device pma291d agoABBOTT MEDICAL — TactiFlex™ Ablation Catheter, Sensor Enabled ™ (TactiFlex SE) (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 30, 2025device pma291d agoMedtronic, Inc. — Avalus Bioprosthesis (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Oct 30, 2025device pma291d agoGuardant Health, Inc. — Shield (PMA supplement)Guardant Health, Inc.

    Supplement type: 30-Day Notice. Product code: PHP. Advisory committee: MG. Decision: OK30

    full page →fda device pma ↗
    ›Oct 30, 2025device pma291d agoMedtronic, Inc. — OmniaSecure™ MRI SureScan™ Lead Model 3930M (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Oct 30, 2025device pma291d agoSiemens Healthcare Diagnostics, Inc. — IMMULITE 2000 AFP (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LOK. Advisory committee: IM. Decision: OK30

    full page →fda device pma ↗
    ›Oct 30, 2025device pma291d agoABBOTT MEDICAL — Epic™, Epic™ Supra, Epic™ Plus, Epic™ Plus Supra and Epic™ Max Stented Tissue Valve (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 30, 2025device pma291d agoSiemens Healthcare Diagnostics, Inc. — IMMULITE 2000 PSA (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MTF. Advisory committee: IM. Decision: OK30

    full page →fda device pma ↗
    ›Oct 30, 2025device recall291d agoCepheid device recall (Cls II)

    Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-10 — Reason: Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 30, 2025device recall291d agoOlympus Corporation of the Americas device recall (Cls I)

    Brand Name: Single Use Ligating Device Product Name: Olympus HX-400U-30 Model/Catalog Number: HX-400U-30 Used with an Olympus endoscope to deliver a nylon loop snare. — Reason: Potential that the ligation loop was unable to release or detach as expected during use, causing the loop to become unintentionally fixed around patient anatomy. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 30, 2025device recall291d agoCepheid device recall (Cls II)

    Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10 — Reason: Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 30, 2025device recall291d agoInpeco S.A. device recall (Cls II)

    FlexLab (FLX); Version: FLX-217-40; — Reason: The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results, this error occurs if the operators open the printer head of mALX to perform error recoveries or maintenance procedures and do not empty the printer tubes buffer to remove all the secondary sample tubes — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 30, 2025device recall291d agoInpeco S.A. device recall (Cls II)

    FlexLab (FLX); Version: FLX-217-10; — Reason: The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results. This error occurs if the operators open the printer head of mALX to perform error recoveries or maintenance procedures and do not empty the printer tubes buffer to remove all the secondary sample tubes. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 31, 2025approval290d agoPENICILLIN V POTASSIUM — FDA approvalNorthstar Rx LLC

    Sponsor: CHARTWELL RX. Form: FOR SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Oct 31, 2025approval290d agoVOQUEZNA TRIPLE PAK (AMOXICILLIN) — FDA approvalamoxicillin + clarithromycin + vonoprazan

    Sponsor: PHATHOM. Form: CAPSULE, TABLET, TABLET. Route: ORAL

    full page →amoxicillin + clarithromycin + vonoprazan →fda approvals ↗
    ›Oct 31, 2025approval290d agoVOQUEZNA DUAL PAK (AMOXICILLIN) — FDA approvalamoxicillin + vonoprazan fumarate

    Sponsor: PHATHOM. Form: CAPSULE, TABLET. Route: ORAL

    full page →amoxicillin + vonoprazan fumarate →fda approvals ↗
    ›Oct 31, 2025approval290d agoPENICILLIN V POTASSIUM — FDA approvalNorthstar Rx LLC

    Sponsor: CHARTWELL RX. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 31, 2025approval290d agoPENICILLIN V POTASSIUM — FDA approvalNorthstar Rx LLC

    Sponsor: CHARTWELL RX. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 31, 2025device 510k290d agoApplied Medical Resources Corp. — Kii Structural Balloon Access System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoApplied Medical Resources Corporation — Voyant® Electrosurgical Generator (EA030/Electrosurgical Generator) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoVigodent Indústria E Comercio Ltda — Hydro Print Premium Fast Set - 454g (1lb) (052037); Hydro Print Premium Regular Set - 454g (1lb) (052327); Chroma Print Premium Fast Set - 454g (1lb) (052457); Chroma Print Premium Regular Set - 454g (1lb) (051460); Perfil Pro - 454g (1lb) (056213); Perfil Pro+ - 454g (1lb) (056121); Perfil Pro Chroma - 454g (1lb) (056122); Hydro Print Premium Fast Set - Multi Pack (056205); Hydro Print Premium Regular Set - Multi Pack (056208); Hydro Print Premium Fast Set - 9,07Kg (20lb) (056204); (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoPhasor Health, LLC — GREEN (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoPropper Manufacturing Co., Inc. — Chex-All Sterilization Pouches and Tubes (510k cleared)Simpson Manufacturing Co., Inc.

    Product code: FRG. Advisory committee: General Hospital. Type: Abbreviated

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoActuated Medical, Inc. — GripTract-GI™ Endoscopic Tissue Manipulator Upper GI Model GT-GS100 (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoPersyst Development, LLC — Persyst 15 EEG Review and Analysis Software (Persyst 15 (P15)) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoCanon Medical Systems Corporation — Aplio i900, Aplio i800 and Aplio i700 Software V9.0 Diagnostic Ultrasound System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoTerrats Medical SL — DESS Dental Smart Solutions (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoOrthofix US, LLC — Firebird SI Navigation System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoBecton, Dickinson and Company — BD Enteric Bacterial Panel for BD COR System, BD Enteric Bacterial Panel plus for BD COR System, and Enteric Bacterial Panel Diluent for BD COR System (510k cleared)BECTON DICKINSON & CO

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoCeribell, Inc. — Ceribell Instant EEG Headcap (Small: C251, Medium: C252) (510k cleared)Ceribell, Inc.

    Product code: GXY. Advisory committee: Neurology. Type: Abbreviated

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoSanhe Meditech Co., Ltd. — Diode Laser Hair Removal Machine (GLD01) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoMedacta International S.A. — MSS - Humeral reverse liners extension (510k cleared)Stemedica International S.A.

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoMaxx Orthopedics, Inc. — Freedom Metaphyseal Cone Implants (Metaphyseal Cones) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 31, 2025device 510k290d agoPulsenmore, Ltd. — Pulsenmore ES (510k cleared)Pulsenmore Ltd.

    Product code: SGJ. Advisory committee: Radiology. Type: Direct

    full page →fda device 510k ↗
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