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calendar

21,836 catalysts · 4,728 grant · 4,110 device 510k · 3,230 8k filing · 3,118 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • device 510k4,110
  • 8k filing3,230
  • approval3,118
  • device pma2,000
  • device recall2,000
device adverse event
1,000
  • recall985
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Mar 10, 2025

    11
    ›Mar 14, 2025device 510k518d agoBaxter Healthcare Corporation — Solution Administration Sets (510k cleared)Baxter Healthcare Corp

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k518d agoArthrex, Inc. — Arthrex 4.75 mm Double Loaded Knotless Corkscrew Suture Anchor (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k518d agoNeurologica Corporation, A Subsidiary of Samsung — BodyTom 64 (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k518d agoMediclus Co., Ltd. — One-Fil Putty (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k518d agoNox Medical Ehf — DeepRESP (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k518d agoPromisemed Hangzhou Meditech Co., Ltd. — Promisemed Safety Huber Needles (510k cleared)

    Product code: PTI. Advisory committee: General Hospital. Type: Special

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k518d agobioMerieux, Inc. — VITEK COMPACT PRO (510k cleared)BIOMERICA INC

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k518d agoMonogram Orthopaedics, Inc. — mBôs (Monogram mBôs TKA System) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k518d agoMoon Surgical — Maestro System (REF100) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k518d agoPenumbra, Inc. — Ruby XL System (510k cleared)Penumbra Inc

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

    full page →fda device 510k ↗
    ›Mar 16, 2025device 510k516d agoContract Medical International, GmbH — Catapult Guide Sheath; 4F; 15cm (US-34015-F-ST-H); Catapult Guide Sheath; 4F; 45cm (US-34045-F-ST-H); Catapult Guide Sheath; 4F; 60cm (US-34060-F-ST-H); Catapult Guide Sheath; 4F; 90cm (US-34090-F-ST-H); Catapult Guide Sheath; 4F; 130cm (US-34130-F-ST-H); Catapult Guide Sheath; 5F; 15cm (US-35015-F-ST-H); Catapult Guide Sheath; 5F; 45cm (US-35045-F-ST-H); Catapult Guide Sheath; 5F; 45cm; Hockey Stick (US-35045-F-HS-H); Catapult Guide Sheath; 5F; 45cm; Multipurpose (US-35045-F-MP-H); Ca (510k cleared)

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

    full page →fda device 510k ↗

    Week of Mar 17, 2025

    39
    ›Mar 17, 2025approval515d agoAMNESTEEM (ISOTRETINOIN) — FDA approvalMylan Pharmaceuticals Inc

    Sponsor: MYLAN PHARMS INC. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Mar 17, 2025approval
    ← prev
    page 19 of 437
    next →
    515d ago
    IMULDOSA (USTEKINUMAB-SRLF) — FDA approvalustekinumab biosimilar

    Sponsor: ACCORD BIOPHARMA INC.. Form: INJECTABLE. Route: INTRAVENOUS

    full page →ustekinumab biosimilar →fda approvals ↗
    ›Mar 17, 2025device 510k515d agoCarlsmed, Inc. — aprevo® anterior and lateral lumbar interbody fusion device, aprevo® anterior lumbar interbody fusion device with interfixation (510k cleared)CARLSMED, INC.

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k515d agoCranial Technologies, Inc. — DOC Band 3D (510k cleared)Q/C TECHNOLOGIES, INC.

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k515d agoLagis Enterprise Co., Ltd. — LAGIS Suction Irrigation System (510k cleared)Cre8 Enterprise Ltd

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k515d agoServ Medical Pte., Ltd. — SERV MEDICAL CDSS (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k515d agoDia Imaging Analysis, Ltd. — LVivo Software Application (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k515d agoJiale Health Technology Shenzhen Co., Ltd. — Air Compression Leg Massager (K-705) (510k cleared)Aimei Health Technology Co., Ltd.

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k515d agoThe Magstim Company Limited — Horizon® 3.0 TMS Therapy System (Horizon 3.0 Inspire); Horizon® 3.0 TMS Therapy System (Horizon 3.0 with StimGuide Pro); Horizon® 3.0 TMS Therapy System (Horizon 3.0) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k515d agoOrthonovis, Inc. — BPS Wrist Fracture System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k515d agoGe Medical Systems, LLC — SIGNA Prime Elite (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k515d agoZiehm Imaging GmbH — Ziehm Solo FD (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k515d agoSpecialty Water Technologies, Inc. — UPT Series Medical RO Water Treatment System (510k cleared)WATTS WATER TECHNOLOGIES INC

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k515d agoCentervue S.P.A. — MAIA (AHMACME001) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoKlarity Medical & Equipment (GZ) Co., Ltd. — Klarity SGRT System (ARSG-E1A, ARSG-E3A) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoWhip Mix Corporation — Hard Splint & Thermo-Adaptive Splint (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoOsteoCentric Technologies — The OsteoCentric Bone Plate and Screw System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoIray Imaging Technology (Haining) Limited — Lux HD 35 Detector (Lux HD 35); Lux HD 43 Detector (Lux HD 43) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoShenzhen Perfect Idea Technology Limited — Aglaia LED Beauty Device (BP-D2309) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoTeleflex Medical — QuikClot Control+ Hemostatic Device (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoVy Spine, LLC — FortiVy™ OsteoVy™ Lumbar IBF (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoBetter Care Plastic Technology Co., Ltd. — Powder Free Nitrile Patient Examination Gloves, Blue Colored, Non Sterile, Low Dermatitis Potential. Tested for Use with Chemotherapy Drugs and Fentanyl Citrate (510k cleared)Teva Pharmaceuticals USA Inc

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoGlobal Healthcare SG Sdn. Bhd — CarbonCool® System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoOlympus Medical Systems Corp. — Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoRadlink, Inc. — Radlink GPS Pro Imaging (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoHangzhou Laihe Biotech Co., Ltd. — LYHER® Oral fluid Multi-Drug Test Kit (Cube) (510k cleared)Hangzhou DAC Biotech Co Ltd

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k514d agoQuibim S.L. — QP-Prostate® CAD (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 19, 2025approval513d agoKEYTRUDA (PEMBROLIZUMAB) — FDA approvalpembrolizumab

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

    full page →pembrolizumab →fda approvals ↗
    ›Mar 19, 2025approval513d agoMEKINIST (TRAMETINIB) — FDA approvalSpexotras

    Sponsor: NOVARTIS. Form: SOLUTION. Route: ORAL

    full page →Spexotras →fda approvals ↗
    ›Mar 19, 2025approval513d agoTAFINLAR (DABRAFENIB MESYLATE) — FDA approvaldabrafenib mesylate ODT

    Sponsor: NOVARTIS. Form: CAPSULE. Route: ORAL

    full page →dabrafenib mesylate ODT →fda approvals ↗
    ›Mar 19, 2025approval513d agoMEKINIST (TRAMETINIB DIMETHYL SULFOXIDE) — FDA approvalSpexotras

    Sponsor: NOVARTIS. Form: TABLET. Route: ORAL

    full page →Spexotras →fda approvals ↗
    ›Mar 19, 2025approval513d agoTAFINLAR (DABRAFENIB MESYLATE) — FDA approvaldabrafenib mesylate ODT

    Sponsor: NOVARTIS. Form: CAPSULE. Route: ORAL

    full page →dabrafenib mesylate ODT →fda approvals ↗
    ›Mar 19, 2025recall513d agoChattem Inc recall (Cls II)Chattem Inc

    Unisom, SleepMelts, Diphenhydramine HCl tablets, 25 mg, Nighttime Sleep-Aid, 4 x 8 blister packs per carton, Cherry flavor, Manufactured by Adare Pharmaceuticals, Inc., Dist. by Chattem, Inc., P.O. Box 2219, Chattanooga, TN 37409, UPC # 0 41167 0014 0 — Reason: CGMP Deviations: Nitrosamine Drug Substance Related Issue impurity above the daily acceptable intake limit defined by the Food and Drug Administration. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 19, 2025recall513d agoAspen Biopharma Labs Pvt., Ltd. recall (Cls II)GlaxoSmithKline LLC

    Chlorambucil Container Description: The product packed in double self-seal cover and finally packed in Aluminum cover for shipping. — Reason: CGMP Deviations — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 19, 2025recall513d agoAspen Biopharma Labs Pvt., Ltd. recall (Cls II)Teva Pharmaceuticals USA Inc

    Finasteride NDC# 82187-1003-1 Container Description: The product packed in white poly bag containing black poly bag and tied each individual finally packed in HDPE container for shipping. — Reason: CGMP Deviations — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 19, 2025recall513d agoKowa Pharmaceuticals America recall (Cls III)Kowa Pharmaceuticals America Inc

    Livalo (pitavatstatin) tablets, 4 mg, 90-count bottles, Rx only, Manufactured by: Patheon, Inc. Cincinnati, OH 45237 USA or by Kowa Company, Ltd, Nagoya, 462-0024 Japan, Marketed by Kowa Pharmaceuticals: Kowa Pharmaceuticals America Inc., Montgomery, AL 36117 USA NDC 66869-404-90 HDPE Bottle, congregated into a shrink wrapped 6-pack further congregated into 24 6-packs in a cardboard case — Reason: Presence of foreign tablets/capsules — Status: Completed

    full page →fda recalls ↗
    ›Mar 19, 2025recall513d agoDenison Pharmaceuticals, LLC recall (Cls II)Dendreon Pharmaceuticals LLC

    Zapzyt, Acne Treatment Gel, 10% benzoyl peroxide Gel, packaged in 1 oz (28.35g) tube, Distributed by: FOCUS CONSUMER HEALTHCARE, LLC., 801 Broad St Ste 200, Chattanooga, TN 37402. NDC 71687-0011-1 — Reason: Chemical Contamination: Presence of benzene. — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 19, 2025recall513d agoJohnson, S C and Son, Inc recall (Cls II)

    Kids by babyganics SPF 50 mineral sunscreen totally tropical (titanium dioxide 3/5%, zinc oxide 7.25%), packaged in 3 OZ spray bottles, Dist. by KAS Direct LLC, 1525 Howe St. Racine, WI 53403, UPC 813277019923 and UPC 813277019916 — Reason: Chemical Contamination — Status: Ongoing

    full page →fda recalls ↗
    ›Mar 19, 2025recall513d agoICU Medical, Inc. recall (Cls I)ICU MEDICAL INC/DE

    POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL, 100 mEq/L flexible container, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26; Bar Code (01)00309907074269 — Reason: Labeling: Label Error on Declared Strength. Overwrap labeled as Potassium Chloride Inj 10 mEq may contain flexible containers of Potassium Chloride Inj 20 mEq — Status: Ongoing

    full page →fda recalls ↗
    $BMRA
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    $ABVC
    $NVS152.24-0.06%
    $NVS152.24-0.06%
    $WTS
    $AFJKU
    $ICUI180.90+0.87%
    $NVS152.24-0.06%
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