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calendar

20,080 catalysts · 4,728 grant · 3,086 8k filing · 3,076 device 510k · 2,774 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • 8k filing3,086
  • device 510k3,076
  • approval2,774
  • device pma2,000
  • device recall2,000
device adverse event
1,000
  • recall751
  • earnings583
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of May 12, 2025

    50
    ›May 12, 2025device 510k457d agoP-Cure, Ltd. — P-Cure Proton Therapy System (PPTS) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 12, 2025device 510k457d agoShanghai United Imaging Healthcare Co., Ltd. — uWS-Angio Basic (510k cleared)

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

    full page →fda device 510k ↗
    ›May 12, 2025device 510k457d agoApyx Medical Corporation — AYON Body Contouring System (AYON SYSTEM) (510k cleared)Apyx Medical Corp

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

    full page →fda device 510k ↗
    ›May 12, 2025device 510k457d agoHeidelberg Engineering GmbH — SPECTRALIS HRA+OCT and variants (510k cleared)

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

    full page →fda device 510k ↗
    ›May 12, 2025device 510k457d ago3D-Side — Archer PSI System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 12, 2025device 510k457d agoInari Medical, Inc. — InThrill™ Thrombectomy System (510k cleared)Mobia Medical, Inc.

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

    full page →fda device 510k ↗
    ›May 13, 2025device 510k456d agoSignature Orthopaedics Pty, Ltd. — Freedom Posterior Cervical Screws (510k cleared)

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

    full page →fda device 510k ↗
    ›May 13, 2025device 510k456d agoIntuitive Surgical, Inc. — SP Endoscope, 0° (430600) (510k cleared)INTUITIVE SURGICAL INC

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

    full page →fda device 510k ↗
    ›May 13, 2025device 510k456d agoCanon Medical Systems Corporation — Aplio i900/i800/i700 Diagnostic Ultrasound System, Software V8.5 (510k cleared)

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

    full page →fda device 510k ↗
    ›May 13, 2025device 510k456d agoUlthera, Inc. — Ulthera System (UC-1 Control Unit PRIME Model 2.1) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 13, 2025device 510k456d agoAesculap, Inc. — Aesculap Aicon® Series Container System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 13, 2025device 510k456d 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 ↗
    ›May 14, 2025approval455d agoKADCYLA (ADO-TRASTUZUMAB EMTANSINE) — FDA approvaltrastuzumab emtansine

    Sponsor: GENENTECH. Form: VIAL. Route: SINGLE-USE

    full page →trastuzumab emtansine →fda approvals ↗
    ›May 14, 2025approval455d agoCAPRELSA (VANDETANIB) — FDA approvalvandetanib

    Sponsor: GENZYME CORP. Form: TABLET. Route: ORAL

    full page →vandetanib →fda approvals ↗
    ›May 14, 2025recall455d agoSiddha Flower Essences, LLC. recall (Cls II)

    temper tamer, 1 US fl oz. (29.6 mL), Homeopathic Oral Spray, Manufactured by: Siddha Flower Essences, Oxnard, CA, 93030 NDC 69779-020-01. — Reason: CGMP Deviations — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoRemedyRePack Inc. recall (Cls II)RemedyRepack Inc

    Clindamycin HCl Capsule, 300 mg, QTY: 30 Capsules per bottle, Rx Only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701. NDC#: 70518-3772-02 — Reason: CGMP Deviations - products manufactured in a shared facility with Ezetimibe tablets. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoBRS Analytical Services, LLC recall (Cls II)

    Artificial Tears Ophthalmic Solution, Dextran 70.01%/Glycerin 0.2%/Hypromellose 0.3% (Eye Lubricants) Lubricant Eye Drops, STERILE, 0.5 FL OZ (15 mL) per dropper bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-043-15. — Reason: cGMP deviations and lack of assurance of sterility. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoFDC Limited recall (Cls II)FDC Ltd

    Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 10mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, NDC 64980-514-01. — Reason: Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoAmneal Pharmaceuticals, LLC recall (Cls I)Amneal Pharmaceuticals, Inc.

    Ropivacaine Hydrochloride Injection, USP, 0.5%, 500 mg per 100 mL (5mg/mL), Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Mehsana, India, , Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807 NDC 70121-1734-1 (bag); NDC 70121-1734-3 (box) — Reason: Presence of Particulate Matter — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoBSO LLC recall (Cls II)Transdermal Delivery Solutions Corp

    TESTOSTERONE PELLET 100 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0101-01 — Reason: Presence of Particulate Matter: Glass particles were found in pellet vials. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoBRS Analytical Services, LLC recall (Cls II)Dr Rajendra Prasad Centre for Ophthalmic Sciences

    Carboxymethylcellulose Sodium Ophthalmic Gel 1%, Carboxymethlycellulose Sodium 1% Eye Lubricant, Lubricant Eye Gel, Soothing Gel, Sterile, 0.5 FL OZ (15mL) per bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-066-15. — Reason: cGMP deviations and lack of assurance of sterility. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoBSO LLC recall (Cls II)Transdermal Delivery Solutions Corp

    TESTOSTERONE PELLET 200 mg BLUNT, 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0121-01 — Reason: Presence of Particulate Matter: Glass particles were found in pellet vials. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoApollo Care, LLC recall (Cls II)Revalesio Corp

    FentaNYL 500mcg (2mcg/mL) and Ropivacaine HCl 250mg (0.1%) added to 250 mL, 0.9% Sodium Chloride Injection (For Epidural Use Only), Sterile, Single-Use Container, Rx Only, Apollocare, 3801 Mojave Ct, Ste 101, Columbia, MO 65202, NDC 71170-950-25 — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoBRS Analytical Services, LLC recall (Cls II)

    Polyvinyl Alcohol Ophthalmic Solution 1.4%, Lubricant Eye Drops, Moisturizing, Sterile, 0.5 FL OZ (15mL) per dropper bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-678-15. — Reason: cGMP deviations and lack of assurance of sterility. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoBSO LLC recall (Cls II)Transdermal Delivery Solutions Corp

    TESTOSTERONE PELLET 200 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0122-01 — Reason: Presence of Particulate Matter: Glass particles were found in pellet vials. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoBRS Analytical Services, LLC recall (Cls II)

    Lubricant Eye Drops Solution, Polyethylene Glycol 400 0.4% Eye Lubricant, Propylene Glycol 0.3% Eye Lubricant, Lubricant Eye Drops, Moisturizing, Sterile, 0.5 FL OZ (15mL) per dropper bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-126-15. — Reason: cGMP deviations and lack of assurance of sterility. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoBSO LLC recall (Cls II)Transdermal Delivery Solutions Corp

    TESTOSTERONE PELLET 200 mg BLUNT (with Cholesterol </=2%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0124-01 — Reason: Presence of Particulate Matter: Glass particles were found in pellet vials. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoBRS Analytical Services, LLC recall (Cls II)Dr Rajendra Prasad Centre for Ophthalmic Sciences

    Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Carboxymethlycellulose Sodium 0.5% Eye Lubricant, Lubricating Eye Drops, Moisturizing, Sterile, 0.5 FL OZ (15mL) per dropper bottle, Distributed by: AvKARE, Pulaski, TN 38478, NDC: 50268-068-15. — Reason: cGMP deviations and lack of assurance of sterility. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025recall455d agoBSO LLC recall (Cls II)Transdermal Delivery Solutions Corp

    TESTOSTERONE PELLET 200 mg (with Cholesterol </=2%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0125-01 — Reason: Presence of Particulate Matter: Glass particles were found in pellet vials. — Status: Ongoing

    full page →fda recalls ↗
    ›May 14, 2025device 510k455d agoTheranica Bio-Electronics, Ltd. — Nerivio; Nerivio Infinity (510k cleared)

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoShenzhen Trious Medical Technology Co., Ltd. — Disposable ureteral stent (510k cleared)NewBay Medical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoTrax Surgical — Linkt Compression Staple System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoShanghai United Imaging Healthcare Co., Ltd. — Medical Image Post-processing Software (uOmnispace.CT) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoZhengzhou PZ Laser Slim Technology Co., Ltd. — Medical Picosecond ND: YAG Laser System (PZ-6) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoWontech Co., Ltd. — Veincare (510k cleared)

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoTribun Health — CaloPix (510k cleared)

    Product code: QKQ. Advisory committee: Pathology. Type: Traditional

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoTaizhou Reach Technology Co., Ltd. — Magnesium alloy scooter (RS100) (510k cleared)Tsuno Rice Fine Chemicals Co Ltd

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoHelios Biomedical, Inc. — Helios Dura Regeneration Matrix (510k cleared)RNR BioMedical Inc

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoCeraroot SL — CeraRoot TL Implant System (TL) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoAscensia Diabetes Care U.S., Inc. — MICROLET®NEXT 2 Lancing Device (510k cleared)

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoEthicon Endo-Surgery, LLC — ETHICON 4000 60mm Compact Stapler (EC3D60C); ETHICON 4000 60mm Standard Stapler (EC3D60S); ETHICON 4000 60mm Long Stapler (EC3D60L); ETHICON 3D 60mm White Reload (ER60W); ETHICON 3D 60mm Blue Reload (ER60B); ETHICON 3D 60mm Green Reload (ER60G); ETHICON 3D 60mm Black Reload (ER60T) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoCube Click, Inc. — Smile Dx® (510k cleared)

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

    full page →fda device 510k ↗
    ›May 14, 2025device 510k455d agoImperative Care, Inc. — Symphony™ Thrombectomy System; Symphony™ 16F 82cm Thrombectomy System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 15, 2025approval454d agoSPRAVATO (ESKETAMINE HYDROCHLORIDE) — FDA approvalJanssen Therapeutics

    Sponsor: JANSSEN PHARMS. Form: SPRAY. Route: NASAL

    full page →fda approvals ↗
    ›May 15, 2025approval454d agoZYNYZ (RETIFANLIMAB-DLWR) — FDA approvalretifanlimab

    Sponsor: INCYTE CORP. Form: INJECTABLE. Route: INTRAVENOUS

    full page →retifanlimab →fda approvals ↗
    ›May 15, 2025device 510k454d agoNIKKISO CO., LTD. — DBB-06 PRO Hemodialysis Delivery System (DBB-06 PRO) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 15, 2025device 510k454d agoStryker Instruments — OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Single Kit); OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Dual Kit) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 15, 2025device 510k454d agoC.R. Bard, Inc. — Bard® Temporary Pacing Electrode Catheter Needle / Cannula (Introducer) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 15, 2025device 510k454d agoNeuraxis — NeurAxis IB-Stim (01-1020) (510k cleared)Neuraxis, INC

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

    full page →fda device 510k ↗
    ›May 15, 2025device 510k454d agoWe Medical Technology (Wuxi) Co., Ltd. — Youmagic FLM System (YM5-U1) (510k cleared)NewBay Medical Technology Co Ltd

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

    full page →fda device 510k ↗
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