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calendar

20,220 catalysts · 4,728 grant · 3,163 device 510k · 3,086 8k filing · 2,805 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • device 510k3,163
  • 8k filing3,086
  • approval2,805
  • device pma2,000
  • device recall2,000
device adverse event
1,000
  • recall773
  • earnings583
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Apr 28, 2025

    50
    ›Apr 30, 2025recall469d agoOurPharma LLC recall (Cls III)SpecGx LLC

    HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL), packaged in a 50 mL Cassette, Rx Only, OurPharma, LLC, 2512 S. City Lake Rd., Fayetteville, AR 72701, NDC 73013-1040-01. — Reason: Superpotent Drug: Assay/potency result for hydromorphone HCl in the compounded stability lot was higher than specification.. — Status: Terminated

    full page →fda recalls ↗
    ›Apr 30, 2025recall469d agoDenver Solutions, LLC DBA Leiters Health recall (Cls II)BioXcel Therapeutics, Inc.

    dexmedeTOMIDine HCl PF, in 0.9% Sodium Chloride, 20 mcg (base) per 5mL, (4 mcg (base) per mL), 5mL Single Dose syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112, NDC: 71449-131-11. — Reason: Lack of Assurance of Sterility: Leaking/damaged syringes. — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 30, 2025recall469d agoLupin Pharmaceuticals Inc. recall (Cls II)LB PHARMACEUTICALS INC

    clomiPRAMINE hydrochloride Capsules USP, 25 mg, 100-count bottle, Rx only, Manufactured For: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, United States, Manufactured By: Lupin Limited, Nagpur, 441 108 INDIA, NDC 68180-492-01 — Reason: Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during 18-month long term stability study. — Status: Terminated

    full page →fda recalls ↗
    ›Apr 30, 2025recall469d agoDenver Solutions, LLC DBA Leiters Health recall (Cls II)Fresenius Kabi USA LLC

    Glycopyrrolate, 1mg per 5mL, (0.2 mg/mL), Single Dose 5 mL syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC 71449-104-11 — Reason: Lack of Assurance of Sterility: Leaking/damaged syringes. — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 30, 2025recall469d agoDenver Solutions, LLC DBA Leiters Health recall (Cls II)NRX Pharmaceuticals, Inc.

    Ketamine HCl 50mg per 5mL (10 mg per mL), 5mL Single Dose Syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112.NDC: 71449-068-11 — Reason: Lack of Assurance of Sterility: Leaking/damaged syringes. — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 30, 2025recall469d agoApipharma recall (Cls II)Grunenthal GmbH

    Kapsin Ointment, Camphor 3.16% and Capsaicin 0.03%. Net Wt. 2 oz (60g) tubes, Manufactured by: Apipharma d.o.o, Jeronima Kavanjina 26, 10090 Zagreb, Croatia, Distributed by: Apipharma, LLC, 2331 West Alameda Drive, Tempe, AZ 85282 UPC 3 858882 101363 — Reason: CGMP Deviations — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 30, 2025recall469d agoDenver Solutions, LLC DBA Leiters Health recall (Cls II)Revalesio Corp

    PHENYLephrine HCl in 0.9% Sodium Chloride, 0.5 mg per 5mL (100 mcg/mL), 5 mL Single Dose Syringe, Rx Only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC: 71449-001-11, — Reason: Lack of Assurance of Sterility: Leaking/damaged syringes. — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 30, 2025recall469d agoPharmadel, LLC recall (Cls II)PharmaDerm LLC

    Rapidol Arnica Tablets, Homeopathic Medicine, 100-count bottle, Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-405-99 — Reason: cGMP deviations — Status: Terminated

    full page →fda recalls ↗
    ›Apr 30, 2025recall469d agoRemedyRepack Inc. recall (Cls II)RemedyRepack Inc

    Clindamycin HCl, 300 mg Capsule, QTY: 30 Capsules per bottle, Rx Only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701. NDC; 70518-3772-00 — Reason: CGMP Deviations — Status: Ongoing

    full page →fda recalls ↗
    ›Apr 30, 2025device 510k469d agoMedivance, Inc. — Arctic Sun Stat Temperature Management System (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoCenterPoint Systems, LLC — AuST Steerable Sheath (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoA.T.S. Applicazione Tecnologie Speciali S.R.L. — Persona C HR (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoSol-Millennium Medical, Inc. — Sol-Guard TM XtraThin Safety Pull-Button Blood Collection Set (510k cleared)

    Product code: JKA. Advisory committee: Clinical Chemistry. Type: Special

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoAidite (Qinhuangdao) Technology Co., Ltd. — Additive Manufacturing (Light Curing) Crown Bridge Resin (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoOptain Health, Inc. — Resolve Fundus Camera (510k cleared)OPKO HEALTH, INC.

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

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoNexus Spine, LLC — Stable-L Lumbar Interbody System (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoCanon Medical Systems Corporation — UltraExtend NX CUW-U001S V2.0 Ultrasound Image Analysis Program (510k cleared)

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

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoContra Healthcare Solutions, LLC — LumiRex Bronchoscope (510k cleared)

    Product code: EOQ. Advisory committee: Ear, Nose, Throat. Type: Traditional

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoAlembic, LLC — APRO 45 Catheter and Alembic Aspiration Tubing (510k cleared)Alembic Pharmaceuticals Inc

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

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoDentsply Sirona — Dentsply Sirona Titanium Bases system (510k cleared)DENTSPLY SIRONA Inc.

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

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoHaemonetics — TEG 6s Hemostasis System Citrated: K, KH, RT, FF Assay Cartridge (510k cleared)HAEMONETICS CORP

    Product code: JPA. Advisory committee: Hematology. Type: Special

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoShenzhen AOJ Medical Technology Co., Ltd. — Arm Blood Pressure Monitor (ARM-30A+);Arm Blood Pressure Monitor (ARM-30G2);Arm Blood Pressure Monitor (ARM-30Q);Arm Blood Pressure Monitor (ARM-30E+); (510k cleared)NewBay Medical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›Apr 30, 2025device 510k469d agoBiomerieux S.A. — ETEST Imipenem/Relebactam P. aeruginosa (IRPA) (0.008/4-128/4 µg/mL) (510k cleared)

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

    full page →fda device 510k ↗
    ›May 1, 2025approval468d agoDEPAKOTE (DIVALPROEX SODIUM) — FDA approvaldivalproex sodium DR

    Sponsor: ABBVIE. Form: CAPSULE, DELAYED REL PELLETS. Route: ORAL

    full page →divalproex sodium DR →fda approvals ↗
    ›May 1, 2025approval468d agoDEPAKOTE ER (DIVALPROEX SODIUM) — FDA approvaldivalproex sodium DR

    Sponsor: ABBVIE. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →divalproex sodium DR →fda approvals ↗
    ›May 1, 2025approval468d agoDEPAKOTE (DIVALPROEX SODIUM) — FDA approvaldivalproex sodium DR

    Sponsor: ABBVIE. Form: TABLET, DELAYED RELEASE. Route: ORAL

    full page →divalproex sodium DR →fda approvals ↗
    ›May 1, 2025approval468d agoTEVIMBRA (TISLELIZUMAB-JSGR) — FDA approvalBeOne Medicines Ltd.

    Sponsor: BEIGENE. Form: INJECTION. Route: SOLUTION

    full page →fda approvals ↗
    ›May 1, 2025approval468d agoTICAGRELOR — FDA approvalTICAGRELOR

    Sponsor: APOTEX. Form: TABLET. Route: ORAL

    full page →TICAGRELOR →fda approvals ↗
    ›May 1, 2025device 510k468d agoOlympus Medical Systems Corp. — Disposable Distal Attachment D-201 Series (510k cleared)

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

    full page →fda device 510k ↗
    ›May 1, 2025device 510k468d agoCepheid® — Xpert Xpress CoV-2/Flu/RSV plus (510k cleared)

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

    full page →fda device 510k ↗
    ›May 1, 2025device 510k468d agoInnovative Sterilization Technologies — ONE TRAY® Sealed Sterilization Container System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 1, 2025device 510k468d agoShenzhen Qianyu Technology Co., Ltd. — Wrinkle Treatment Device (JM1, JM2B) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

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

    full page →fda device 510k ↗
    ›May 1, 2025device 510k468d agoAlembic, LLC — APRO 45 Catheter (510k cleared)Alembic Pharmaceuticals Inc

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

    full page →fda device 510k ↗
    ›May 1, 2025device 510k468d agoParagon 28, Inc. — APEX 3D Total Ankle Replacement System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 1, 2025device 510k468d agoCepheid® — Xpert Xpress CoV-2/Flu/RSV plus (510k cleared)

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

    full page →fda device 510k ↗
    ›May 1, 2025device 510k468d agoTraferox Technologies, Inc. — X°Port Lung Preservation System; X°Port Lung Preservation Solution (510k cleared)TETRA TECHNOLOGIES INC

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

    full page →fda device 510k ↗
    ›May 1, 2025device 510k468d agoBioHorizons Implant Systems, Inc. — Conical Ti Base abutments (510k cleared)

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

    full page →fda device 510k ↗
    ›May 1, 2025device 510k468d agoUnited Orthopedic Corporation — Resolve Modular Revision Hip Stem (510k cleared)

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

    full page →fda device 510k ↗
    ›May 1, 2025device 510k468d agoCirca Scientific, Inc. — CrossWise RF Transseptal Access System (Models: CW-1085S, CW-1085A, CW-1012W, CW-1012C, CW-1085C, CW-1085V, CW-1013F) (510k cleared)Clear Scientific Inc

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

    full page →fda device 510k ↗
    ›May 1, 2025device 510k468d agoGE Medical Systems Ultrasound and Primary Care Diagnostics — Vscan Air (510k cleared)

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

    full page →fda device 510k ↗
    ›May 2, 2025approval467d agoTICAGRELOR — FDA approvalTICAGRELOR

    Sponsor: ALEMBIC. Form: TABLET. Route: ORAL

    full page →TICAGRELOR →fda approvals ↗
    ›May 2, 2025device 510k467d agoPfm Medical, Inc. — JetCan® Pro Safety Huber Needle (510k cleared)Picard Medical, Inc.

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

    full page →fda device 510k ↗
    ›May 2, 2025device 510k467d agoShockwave Medical, Inc. — Shockwave CS Guide Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›May 2, 2025device 510k467d agoHathor Professional Skincare , Ltd. — Sutil Rich Personal Lubricant (510k cleared)

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

    full page →fda device 510k ↗
    ›May 2, 2025device 510k467d agoSignature Orthopaedics Pty, Ltd. — Origin™ Cemented Hip Stem (510k cleared)

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

    full page →fda device 510k ↗
    ›May 2, 2025device 510k467d agoBeijing Rongrui-Century Science & Technology Co., Ltd. — SpO2 Extension Cable (510k cleared)

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

    full page →fda device 510k ↗
    ›May 2, 2025device 510k467d agoAbbott Point of Care, Inc. — i-STAT CG4+ cartridge with the i-STAT 1 System (510k cleared)

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

    full page →fda device 510k ↗
    ›May 2, 2025device 510k467d agoSg Endoscopy Pte, Ltd. — F88 URE-SD/RD Flexible Ureteroscope (510k cleared)

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

    full page →fda device 510k ↗
    ›May 2, 2025device 510k467d agoSTERIS Corporation — Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118 (510k cleared)STERIS plc

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

    full page →fda device 510k ↗
    ›May 2, 2025device 510k467d agoSeriously Clean, Ltd. — Nixall Antimicrobial Solutions™ Skin & Wound Hydrogel (510k cleared)

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

    full page →fda device 510k ↗
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    $OPK1.39000.00%
    $BTAI0.9215-10.53%
    $ABBV247.97+0.78%
    $LBRX45.52-0.72%
    $NRXP
    $HAE
    $XRAY11.70+0.34%
    $ONC361.49+0.69%
    $ABBV247.97+0.78%
    $ABBV247.97+0.78%
    $TTI
    $PMI0.1821-4.66%
    $FRTRY
    $STE239.63+0.30%