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23,486 catalysts · 5,000 device 510k · 4,728 grant · 3,778 approval · 3,189 8k filing · 2,000 device pma · 2,000 device recall

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  • device 510k5,000
  • grant4,728
  • approval3,778
  • 8k filing3,189
  • device pma2,000
  • device recall2,000
recall
1,126
  • device adverse event1,000
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Nov 11, 2024

    1
    ›Nov 15, 2024device 510k636d agoLivsmed, Inc. — ArtiSeal Vessel Sealing System-ArtiSeal Instruments; ArtiSeal Vessel Sealing System-ArtiSeal Generator (510k cleared)

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

    full page →fda device 510k ↗

    Week of Nov 18, 2024

    49
    ›Nov 18, 2024device 510k633d agoMindset Medical, Inc. — Informed Vital Core Application (IVC App) (510k cleared)Outset Medical, Inc.

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

    full page →fda device 510k ↗
    ›Nov 18, 2024device 510k633d agoSorin Group Italia S.R.L. — MICRO Arterial Filters (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 18, 2024device 510k633d agoZhejiang Innuovo Rehabilitation Devices Co.,Ltd — Power Wheelchair (W5538) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 18, 2024device 510k633d agoOrthocon, Inc. — Montage-XT Settable Bone Putty (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 18, 2024device 510k633d agoZhejiang Zhonglei Medical Technology Co. , Ltd. — Power wheelchair (510k cleared)Zhejiang Xinkanghe Biomedical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›Nov 18, 2024device 510k633d agoTrice Medical, Inc. — Tenex 2nd Generation System (510k cleared)Tenon Medical, Inc.

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

    full page →fda device 510k ↗
    ›Nov 18, 2024device 510k633d agoDeepHealth, Inc. — Saige-Dx (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 18, 2024device 510k633d agoXiamen Weiyou Intelligent Technology Co., Ltd. — Air Pressure Therapy System (VU-IPC04B) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 18, 2024device 510k633d agoHebei Keylaser Sci-Tech Co.,Ltd — Diode laser Treatment System (K18) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 18, 2024device 510k633d agoEnlight Medical Technologies (Shenzhen) Co., Ltd. — Synxess Neurovascular Guidewire (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 18, 2024device 510k633d agoIntuitive Surgical, Inc. — da Vinci SP Instruments (SP1098) (510k cleared)INTUITIVE SURGICAL INC

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

    full page →fda device 510k ↗
    ›Nov 18, 2024device 510k633d agoPhilips Healthcare (Suzhou) Co., Ltd. — CT Collaboration Live (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2024approval632d agoQSYMIA (PHENTERMINE HYDROCHLORIDE) — FDA approval(phentermine hydrochloride + topiramate) ER

    Sponsor: VIVUS LLC. Form: CAPSULE, EXTENDED RELEASE. Route: ORAL

    full page →(phentermine hydrochloride + topiramate) ER →fda approvals ↗
    ›Nov 19, 2024approval632d agoPAXLOVID (COPACKAGED) (NIRMATRELVIR) — FDA approvalPAXLOVID (COPACKAGED)

    Sponsor: PFIZER. Form: TABLET. Route: ORAL

    full page →PAXLOVID (COPACKAGED) →fda approvals ↗
    ›Nov 19, 2024device 510k632d agoCerrozone, LLC — CerroZone Mini (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoNova Biomedical Corporation — Nova Allegro UACR Assay, Nova Allegro Analyzer (510k cleared)

    Product code: CGX. Advisory committee: Clinical Chemistry. Type: Dual Track

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoMaxx Orthopedics, Inc. — Freedom® Medial Congruent Liner (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoPolarean, Inc. — XENOVIEW 3.0T Chest Coil (510k cleared)Polaris Inc.

    Product code: MOS. Advisory committee: Radiology. Type: Special

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoRiverpoint Medical — Iconix Knotless Anchor (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoDongguanshi Yiyingmei Technology Co., Ltd. — Nasal Aspirator (BC-021, BC-022, BC-023, BC-024, BC-025, BC-026) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoEieling Technology (Shenzhen) Limited — Portable Liver Elastography Ultrasound Diagnostic System (Liverscan C) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoBraxx Biotech Co., Ltd. — “BRAXX” Esophageal Brachytherapy Applicator (Model: BKMI2001, BKMI2002) (510k cleared)

    Product code: JAQ. Advisory committee: Radiology. Type: Special

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoTaidoc Technology Corporation — XPER Technology PREMIUM Pro Blood Glucose Monitoring System (510k cleared)

    Product code: PZI. Advisory committee: Clinical Chemistry. Type: Dual Track

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoRhein Laser Technologies Co., Ltd. — Medical Thulium Fiber Laser Systems (UroFiber 60Q) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoMiRus, LLC — EUROPA™ Posterior Cervical Fusion System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoNatus Medical Incorporated Dba Excel-Tech Ltd. (Xltek) — Natus BrainWatch System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2024device 510k632d agoSiemens Medical Solutions USA, Inc. — ACUSON Sequoia Diagnostic Ultrasound System; ACUSON Sequoia Select Diagnostic Ultrasound System; ACUSON Origin Diagnostic Ultrasound System; ACUSON Origin ICE Diagnostic Ultrasound System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2024approval631d agoKEYTRUDA (PEMBROLIZUMAB) — FDA approvalpembrolizumab

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

    full page →pembrolizumab →fda approvals ↗
    ›Nov 20, 2024approval631d agoADRENACLICK (EPINEPHRINE) — FDA approvalViatris Inc

    Sponsor: IMPAX. Form: INJECTABLE. Route: INTRAMUSCULAR, SUBCUTANEOUS

    full page →fda approvals ↗
    ›Nov 20, 2024approval631d agoOXYCODONE AND ACETAMINOPHEN (ACETAMINOPHEN) — FDA approvalIGC Pharma, Inc.

    Sponsor: SANALUZ. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 20, 2024approval631d agoHYDROCODONE BITARTRATE AND ACETAMINOPHEN (ACETAMINOPHEN) — FDA approvalIGC Pharma, Inc.

    Sponsor: SANALUZ. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 20, 2024recall631d agoThe Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recall (Cls III)Teva Pharmaceuticals USA Inc

    Hydralazine HCl Tablets, USP, 25mg, Rx only, 100 tablets per carton, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816, Distributed by: MAJOR Pharmaceuticals, Livonia, MI, 48152, USA, NDC 0904-6441-61. — Reason: Failed Impurities/Degradation Specifications; during routine stability testing for impurities. — Status: Terminated

    full page →fda recalls ↗
    ›Nov 20, 2024recall631d agoCipla USA, Inc. recall (Cls II)Cipla USA Inc

    Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Cipla USA, NDC 69097-0936-98 — Reason: Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 20, 2024recall631d agoTrinity Gold Nutrition recall (Cls II)IGC Pharma, Inc.

    Trinity Gold Nutrition, 60 Capsule, 30 day Supply, Distributed by Trinity Gold Nutrition 201 Tom Hall St. Ste. 2107, Fortmill, SC 29716, USA, Ph: 704-629-8203, www.trinitygold.com, Made in India, UPC 802992001009 — Reason: Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac and phenylbutazone. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 20, 2024recall631d agoKeystone Industries recall (Cls II)

    Perio Maintenance Rinse 0.63% Stannous Fluoride Concentrated Solution, Rx Only, Net Wt. 10 oz. (283.5 g) pumps, Mint flavor, Manufactured by: Keystone Industries, 480 S. Democrat Rd., Gibbstown, NJ 08027, NDC 68400-202-10 — Reason: Subpotent Drug — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 20, 2024recall631d agoCipla USA, Inc. recall (Cls II)Cipla USA Inc

    Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Exelan Pharmaceuticals, NDC 76282-0478-90 — Reason: Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 20, 2024device 510k631d agoSmith & Nephew, Inc. — AETOS Shoulder System Stemless Humeral Prosthesis (510k cleared)SMITH & NEPHEW PLC

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

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoEterbio, Inc. — ETERBIO Fentanyl/Norfentanyl Rapid Test (Colloidal Gold); ETERBIO Fentanyl/Norfentanyl Home Test (510k cleared)NutriBand Inc.

    Product code: NGL. Advisory committee: Clinical Toxicology. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoOsartis GmbH — Hip Spacer Molds; Knee Spacer Molds; Shoulder Spacer Molds (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoSol-Millennium Medical, Inc. — SOL-M Luer Lock Syringe (Low Dead Space) w/o Needle, SOL-M Slip Tip Syringe (Low Dead Space) w/o needle, SOL-M Luer Lock Syringe (Low Dead Space) w/Exchangeable Needle, SOL-CARE Luer Lock Syringe (Low Dead Space) w/Safety Needle, SOL-M Slip Tip Syringe (Low Dead Space) w/Exchangeable Needle (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoPenumbra, Inc. — Element Vascular Access System (510k cleared)Penumbra Inc

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

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoZhejiang Nysin Medical Co., Ltd. — Powered Wheelchair (NXN20-208, NXN20-211) (510k cleared)Zhejiang Medicine Co Ltd

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

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoIndiba S. A. U. — INDIBA COMPACT devices (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoPro Surgical, Inc. — ProAM ACDF System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoOsstem Implant Co., Ltd. — Estar-ZE (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoExo, Inc. — Strain AI (SAI001) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoShenzhen Ruiyi Business Technology Co., Ltd. — Leg Massager (Models:RP-ALM070H, RP-ALM071H) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoGostar Co., Ltd. — TD-7301 Spirometer (TD-7301) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2024device 510k631d agoQ'Apel Medical, Inc. — Neurovascular Access System Family (510k cleared)

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

    full page →fda device 510k ↗
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    $PII68.52-2.24%
    $PFE26.31-1.16%
    $VTRS16.10-1.11%
    $ISRG401.27+0.01%
    $OM4.5200-1.09%
    $TNON0.2832-3.11%
    $IGC0.2670+0.41%
    $SNN29.84-0.57%
    $NTRB2.9000-11.59%
    $PEN324.29-0.11%
    $IGC0.2670+0.41%
    $IGC0.2670+0.41%