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21,500 catalysts · 4,728 grant · 3,844 device 510k · 3,286 8k filing · 3,046 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • device 510k3,844
  • 8k filing3,286
  • approval3,046
  • device pma2,000
  • device recall2,000
device adverse event
1,000
  • recall931
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Apr 7, 2025

    24
    ›Apr 11, 2025approval490d agoCABENUVA KIT (CABOTEGRAVIR) — FDA approvalViiV Healthcare Company

    Sponsor: VIIV HLTHCARE. Form: SUSPENSION, EXTENDED RELEASE. Route: INTRAMUSCULAR

    full page →fda approvals ↗
    ›Apr 11, 2025device 510k490d agoFoshan Coxo Medical Instrument Co., Ltd. — LED Curing Lights (DB686 HALO) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoNelson Environmental Technologies, Inc. — Chlorine Sentinel II (510k cleared)BION ENVIRONMENTAL TECHNOLOGIES INC

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoOncospace, Inc. — Oncospace (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoSmartsurgN, Inc. — AirSurgN Insufflator (10030/AirSurgN) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoShenzhen Trious Medical Technology Co., Ltd. — Disposable ureteral access sheath (510k cleared)NewBay Medical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoAlma Lasers, Inc. — Alma Harmony (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoFujifilm Corporation — FUJIFILM Processor EP-8000; FUJIFILM Endoscope Model EG-860R (510k cleared)Fujifilm Holdings Corp

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoXelite Biomed , Ltd. — XeliteMed VertehighFix High Viscosity Spinal Bone Cement System (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoCognoa, Inc. — Canvas Dx (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoGuilin Aesthedent Medical Instruments Co., Ltd. — Dental Implant Unit (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoDentsply Sirona — Atlantis® Abutments in Titanium (510k cleared)DENTSPLY SIRONA Inc.

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoShenzhen Vivolight Medical Device & Technology Co., Ltd. — Cornaris Intravascular Imaging System (P80-E); Cornaris Intravascular Imaging System (Mobile-E); LumenCross Imaging Catheter (F2) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoKlaxon-Mobility GmbH — KLAXON (TWIST); KLAXON (TWIST R) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoCooperSurgical, Inc. — CooperSurgical Milex® Pessaries (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoAidite (Qinhuangdao) Technology Co., Ltd. — Dental Zirconia Ceramic (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoAsiga Pty, Ltd. — Asiga DentaBASE (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoShanghai AnQing Medical Instrument Co., Ltd. — Flexible Ureterorenoscope (US27F-12-EU; US27F-12-US) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoCascination AG — OTOPLAN (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoClick Therapeutics, Inc. — CT-132 (510k cleared)Click Holdings Ltd.

    Product code: SEE. Advisory committee: Neurology. Type: Direct

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoPearl, Inc. — Second Opinion Periapical Radiolucency Contours (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoRoche Molecular Systems, Inc. — cobas liat SARS-CoV-2 v2 nucleic acid test (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoMedline Industries, LP — Medline UNITE® REFLEX® Hybrid Nitinol Implant System (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 11, 2025device 510k490d agoGalileo Cds, Inc. — GBrain MRI (510k cleared)

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

    full page →fda device 510k ↗

    Week of Apr 14, 2025

    26
    ›Apr 14, 2025approval487d agoOTULFI (USTEKINUMAB-AAUZ) — FDA approvalOTULFI

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

    full page →OTULFI →fda approvals ↗
    ›Apr 14, 2025approval
    ← prev
    page 19 of 430
    next →
    487d ago
    ACETAMINOPHEN, CAFFEINE AND DIHYDROCODEINE BITARTRATE (ACETAMINOPHEN) — FDA approvalIGC Pharma, Inc.

    Sponsor: PHARMOBEDIENT. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Apr 14, 2025device 510k487d agoElfi-Tech , Ltd. — Elfor-L (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 14, 2025device 510k487d agoMediclus Co., Ltd. — Any-Com Flow (510k cleared)

    Product code: EBF. Advisory committee: Dental. Type: Special

    full page →fda device 510k ↗
    ›Apr 14, 2025device 510k487d agoNeuralynx, Inc. — Atlas Stim Headbox (NK) (31-0601-0077); Atlas Stim Headbox (Touchproof) (31-0601-0089); Atlas Stim Headbox (HD) (31-0601-0132); ASHB FIBER OPTIC DUPLEX CONN 2m (31-0204-0001); ASHB FIBER OPTIC DUPLEX CONN 7m (31-0204-0002); ATLAS Stim Headbox Software (36-0301-0006); Atlas Headbox Interface Cable (NK) (31-0204-003); Atlas Headbox Interface Cable (Touchproof) (31-0204-004); Atlas Headbox Interface Cable (HD) (31-0204-005); Atlas Headbox Expansion Panel (31-0607-0014) (510k cleared)Neuraly Inc

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

    full page →fda device 510k ↗
    ›Apr 14, 2025device 510k487d agoMerge Healthcare Incorporated — Merge Universal Viewer (MUV) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 14, 2025device 510k487d agoAVAVA, Inc. — AVAVA™ Skin Treatment System (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 14, 2025device 510k487d agoAdvanced Sterilization Products, Inc. — STERRAD® 100NX Sterilizer with ALLClear™ Technology (10104) (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 15, 2025approval486d agoISTURISA (OSILODROSTAT PHOSPHATE) — FDA approvalosilodrostat phosphate

    Sponsor: RECORDATI RARE. Form: TABLET. Route: ORAL

    full page →osilodrostat phosphate →fda approvals ↗
    ›Apr 15, 2025approval486d agoTICAGRELOR — FDA approvalAstraZeneca Pharmaceuticals LP

    Sponsor: SUNSHINE. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Apr 15, 2025device 510k486d agoEMA Aesthetics , Ltd. — Préime DermaFacial Collagen+ (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 15, 2025device 510k486d agoCryoconcepts LP — Skin Clinic Nitro Clear Wart Remover (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 15, 2025device 510k486d agoThermo Fisher Scientific — The Sensititre 18-24 hour MIC or Breakpoint Susceptibility System with Moxifloxacin in the dilution range of 0.008-16 ug/mL (510k cleared)THERMO FISHER SCIENTIFIC INC.

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

    full page →fda device 510k ↗
    ›Apr 15, 2025device 510k486d agoArineta , Ltd. — SpotLight / SpotLight Duo with Low Dose Lung Cancer Screening Option (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 15, 2025device 510k486d agoSight Sciences, Inc. — TearCare MGX System (510k cleared)Sight Sciences, Inc.

    Product code: ORZ. Advisory committee: Ophthalmic. Type: Traditional

    full page →fda device 510k ↗
    ›Apr 15, 2025device 510k486d agoBoston Scientific Corporation — Percuflex Ureteral Stent; Percuflex Plus Ureteral Stent; Percuflex Plus SureDrive Steerable Ureteral Stent Set; Contour Ureteral Stent; Contour SureDrive Steerable Ureteral Stent Set; Contour VL Variable Length Ureteral Stent; Contour VL SureDrive Steerable Ureteral Stent Set; Polaris Ultra Ureteral Stent; Polaris Loop Ureteral Stent; Tria Firm Ureteral Stent; Tria Soft Ureteral Stent; Percuflex Urinary Diversion Stent Set (510k cleared)BOSTON SCIENTIFIC CORP

    Product code: FAD. Advisory committee: Gastroenterology, Urology. Type: Special

    full page →fda device 510k ↗
    ›Apr 15, 2025device 510k486d agoAnhui Deepblue Medical Technological Co., Ltd. — Deepblue Multi-Drug Urine Test Cup; Deepblue Home Muti-Drug Urine Test Cup (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 15, 2025device 510k486d agoGeistlich Pharma AG — SwissMembrane X; SwissMembrane X Socket (510k cleared)

    Product code: NPL. Advisory committee: Dental. Type: Special

    full page →fda device 510k ↗
    ›Apr 15, 2025device 510k486d agoArk Surgical — LapBox Power Tissue Containment System (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 15, 2025device 510k486d agoStryker Instruments — OptaBlate Radiofrequency (RF) Generator System (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 15, 2025device 510k486d agoSteris — Electro Lube NXT (510k cleared)STERIS plc

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

    full page →fda device 510k ↗
    ›Apr 16, 2025approval485d agoDUPIXENT (DUPILUMAB) — FDA approvaldupilumab

    Sponsor: REGENERON PHARMACEUTICALS. Form: INJECTABLE. Route: INJECTION

    full page →dupilumab →fda approvals ↗
    ›Apr 16, 2025approval485d agoCARBAMAZEPINE — FDA approvalcarbamazepine ER

    Sponsor: ALEMBIC. Form: TABLET. Route: ORAL

    full page →carbamazepine ER →fda approvals ↗
    ›Apr 16, 2025recall485d agoSomerset Therapeutics Private Limited recall (Cls II)Somerset Therapeutics LLC

    Haloperidol Decanoate Injection 50mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured by: Somerset Therapeutics Limited, Kamataka India, Manufactured for: BluePoint Laboratories NDC 68001-580-41 — Reason: Lack of Assurance of Sterility: Media fill with bacterial contamination — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 16, 2025recall485d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

    Cetirizine Hydrochloride Tablets, USP, 10mg, 365-count packs, Rx Only, Manufactured for: Glenmark Therapeutics Inc., Distributed by: Amazon. NDC# 72657-129-35 — Reason: CGMP Deviations — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 16, 2025recall485d agoASEGUA THERAPEUTICS LLC recall (Cls II)Asegua Therapeutics LLC

    Sofosbuvir and Velpatasvir, 400 mg/100 mg tablets, 28 tablets: 2x14 blister cards, Rx Only, Manufactured for: Asegua Therapeutics LLC an affiliate of Gilead Sciences, Inc., Foster City, CA 94404, Made in Ireland, NDC# 72626-2701-1 — Reason: Defective Container: blister packs not properly sealed resulting in tablets being loose in the carton. — Status: Ongoing

    full page →fda recalls ↗
    $BNET
    $CLIK
    $XRAY11.48+0.61%
    $LBRX45.02-0.79%
    $SGHT5.0300+2.44%
    $REGN812.08+1.77%
    $STE235.15-0.61%
    $TMO447.81+1.31%
    $IGC0.2670+0.41%
    $BSX51.39-0.07%