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18,412 catalysts · 4,728 grant · 3,404 8k filing · 2,627 approval · 2,156 device 510k · 1,745 device recall · 1,501 device pma

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  • grant4,728
  • 8k filing3,404
  • approval2,627
  • device 510k2,156
  • device recall1,745
  • device pma1,501
device adverse event
1,000
  • recall586
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
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    Week of Sep 15, 2025

    50
    ›Sep 19, 2025approval334d agoDIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE (ATROPINE SULFATE) — FDA approvalANI PHARMACEUTICALS INC

    Sponsor: ANI PHARMS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Sep 19, 2025approval334d agoGABAPENTIN — FDA approvalSciegen Pharmaceuticals Inc

    Sponsor: SCIEGEN PHARMS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Sep 19, 2025approval334d agoLOSARTAN POTASSIUM — FDA approvalGraviti Pharmaceuticals Inc

    Sponsor: GRAVITI PHARMS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Sep 19, 2025approval334d agoPROPOFOL — FDA approvalPROPOFOL

    Sponsor: HOSPIRA. Form: INJECTABLE. Route: INJECTION

    full page →PROPOFOL →fda approvals ↗
    ›Sep 19, 2025device 510k334d agoIbramed Equipamentos Médicos — VEGA (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoMedacta International S.A. — Coated hip implants (510k cleared)Stemedica International S.A.

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoBunkerHill Health — Bunkerhill ECG-EF (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoMedica USA, Inc. — Purema H Hemoconcentrator - Pediatric (510k cleared)Medunik USA Inc

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoShanghai United Imaging Healthcare Co., Ltd. — uDR Aurora CX (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoTempus AI, Inc. — xR IVD (510k cleared)Tempus AI, Inc.

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoOptmed, Inc. — BondEase 2 Topical Skin Adhesive (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoOlympus Medical Systems Corp. — EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V (TJF-Q190V) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoIpg Medical Corporation — IPGTFL-02 (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoHuntleigh Healthcare , Ltd. — Sonicaid Team3 (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoNakanishi, Inc. — UniBur (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoAnhui Happiness Workshop Medical Instruments Co., Ltd. — Single Use Suction-Evacuation Ureteral Access Sheath (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoVideahealth, Inc. — Videa Dental AI (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoShenzhen Jermei Medical Device Technology Co., Ltd. — Portable mesh nebulizer (JM821) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoEmbody, Inc. — Tapestry Biointegrative Implant (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoGC America, Inc. — EQUIA LC ONE (510k cleared)PARKS AMERICA, INC

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoVericom Co., Ltd. — Well-Root PT (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoNvision Biomedical Technologies, Inc. — Impact PEEK Union Nail System (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoUnibeauty (Hubei) Technology Co., Ltd. — Unscented menstrual three-piece applicator tampon (510k cleared)

    Product code: HEB. Advisory committee: Obstetrics/Gynecology. Type: Special

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoNakanishi, Inc. — VARIOS 170 LUX SCALER SYSTEM (VA170LUXS10); VARIOS 170 LUX SCALER SYSTEM (VA170LUXS11); VARIOS 170 SCALER SYSTEM (VA170S11) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoZeus Scientific — Alegria Flash ENA Screen (510k cleared)Dawn Sea Therapeutics

    Product code: LLL. Advisory committee: Immunology. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 19, 2025device 510k334d agoCytocell Limited — KMT2A Breakapart FISH Probe Kit PDx (CDA-LPH013) (510k cleared)

    Product code: SFS. Advisory committee: Hematology. Type: Direct

    full page →fda device 510k ↗
    ›Sep 19, 2025device pma334d agoBoston Scientific Corp — Vercise Deep Brain Stimulation (DBS) Systems (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: NHL. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Sep 19, 2025device pma334d agoAbiomed, Inc. — Impella RP, Impella RP with SmartAssist, Impella RP Flex with SmartAssist (PMA supplement)Abion Inc

    Supplement type: 30-Day Notice. Product code: PYX. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Sep 19, 2025device pma334d agoContego Medical, Inc. — Neuroguard IEP® 3-in-1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection – (Neuroguard I (PMA supplement)

    Supplement type: 30-Day Notice. Product code: NIM. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Sep 19, 2025device pma334d agoRoche Molecular Systems, Inc. — cobas HPV (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: MAQ. Advisory committee: MI. Decision: APPR

    full page →fda device pma ↗
    ›Sep 19, 2025device pma334d agoBoston Scientific Corp — Carotid Wallstent™ Monorail™ Endoprosthesis (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: Special (Immediate Track). Product code: NIM. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Sep 19, 2025device pma334d agoIllumina, Inc. — TruSight Oncology Comprehensive (PMA supplement)ILLUMINA, INC.

    Supplement type: 30-Day Notice. Product code: PQP. Advisory committee: PA. Decision: OK30

    full page →fda device pma ↗
    ›Sep 19, 2025device pma334d agoOrganox Limited — OrganOx metra® System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: QQK. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Sep 19, 2025device pma334d agoRoche Molecular Systems, Inc. — cobas HBV (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: MKT. Advisory committee: MI. Decision: APPR

    full page →fda device pma ↗
    ›Sep 19, 2025device pma334d agoMedtronic, Inc. — Sphere-9 Catheter and Affera Ablation System (PMA supplement)Medtronic plc

    Supplement type: 30-Day Notice. Product code: QZI. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Sep 19, 2025device pma334d agoBoston Scientific Corp — Precision Spinal Cord Stimulator (SCS) Systems (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: LGW. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Sep 19, 2025device pma334d agoAbiomed, Inc. — Impella 2.5; Impella CP; Impella CP with SmartAssist; Impella 5.0; Impella 5.5 with SmartAssist; Impella LD (PMA supplement)Abion Inc

    Supplement type: 30-Day Notice. Product code: OZD. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Sep 19, 2025device recall334d agoKico Knee Innovation Company device recall (Cls II)

    Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software Software Version: V2025.1.2 Product Description: Intended Use: The ARVIS" system is a computer-controlled navigation system intended to provide intra-operative measurements to the surgeon to aid in selection and positioning of orthopedic implant components. Description: ARVIS Shoulder is a computer-controlled surgical navigation system for shoulder arthroplasty. It aids the surgeon in making intra-operative measurements and locating anatomical structures of the shoulder joint based on the patient s preoperative imaging to assist with selection and positioning of orthopedic implant components. The system consists of software, electronic hardware and surgical instruments. The device s workflow involves CT based preoperative planning followed by intraoperative navigation and execution. The preoperative planning software enables 3D virtual implant positioning based on the patient s CT reconstructed digital bone model and bony landmarks. The shoulder navigation application software then matches the patient s digital bone model and landmarks to the intraoperative landmarks registered by the surgeon, allowing an image-based navigation to follow. The surgeon uses the plan data as guidance to navigate and help position shoulder instruments and implants. — Reason: Complaint identified issue with AI surgical planning software that may result in implant malalignment and/or decrease range of motion. — Status: Ongoing

    full page →
    ›Sep 19, 2025device recall334d agoBeckman Coulter, Inc. device recall (Cls II)

    DxI 9000 Access Immunoassay Analyzer, Part Number C11137 — Reason: Beckman Coulter has confirmed a software anomaly on DxI 9000 Access Immunoassay Analyzer and the DxC 500i Clinical Analyzer that may prevent correct application of user-specified manual dilution factors when ordering additional tests for samples already "In Progress" using the same "Sample ID number". This can lead to false low or high patient results and potential delays in reporting, risking erroneous diagnoses if undetected. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 19, 2025device recall334d agoOrthofix U.S. LLC device recall (Cls II)

    Virata Preassembled Polyaxial Screw, utilized in the Virata Spinal Fixation System. The following sizes are affected: 1. POLYAXIAL SCREW, CC, 5.5mm X 30mm; Item Number: TL1-10755030. 2. POLYAXIAL SCREW, CC, 5.5mm X 35mm; Item Number: TL1-10755035. 3. POLYAXIAL SCREW, CC, 5.5mm X 40mm; Item Number: TL1-10755040. 4. POLYAXIAL SCREW, CC, 5.5mm X 45mm; Item Number: TL1-10755045. 5. POLYAXIAL SCREW, CC, 5.5mm X 50mm; Item Number: TL1-10755050. 6. POLYAXIAL SCREW, CC, 6.5mm X 30mm; Item Number: TL1-10765030. 7. POLYAXIAL SCREW, CC, 6.5mm X 35mm; Item Number: TL1-10765035. 8. POLYAXIAL SCREW, CC, 6.5mm X 40mm; Item Number: TL1-10765040. 9. POLYAXIAL SCREW, CC, 6.5mm X 45mm; Item Number: TL1-10765045. 10. POLYAXIAL SCREW, CC, 6.5mm X 50mm; Item Number: TL1-10765050. 11. POLYAXIAL SCREW, CC, 6.5mm X 55mm; Item Number: TL1-10765055. 12. POLYAXIAL SCREW, CC, 6.5mm X 60mm; Item Number: TL1-10765060. 13. POLYAXIAL SCREW, CC, 7.5mm X 30mm; Item Number: TL1-10775030. 14. POLYAXIAL SCREW, CC, 7.5mm X 35mm; Item Number: TL1-10775035. 15. POLYAXIAL SCREW, CC, 7.5mm X 40mm; Item Number: TL1-10775040. 16. POLYAXIAL SCREW, CC, 7.5mm X 45mm; Item Number: TL1-10775045. 17. POLYAXIAL SCREW, CC, 7.5mm X 50mm; Item Number: TL1-10775050. 18. POLYAXIAL SCREW, CC, 7.5mm X 55mm; Item Number: TL1-10775055. 19. POLYAXIAL SCREW, CC, 7.5mm X 60mm; Item Number: TL1-10775060. 20. POLYAXIAL SCREW, CC, 8.5mm X 35mm; Item Number: TL1-10785035. 21. POLYAXIAL SCREW, CC, 8.5mm X 40mm; Item Number: TL1-10785040. 22. POLYAXIAL SCREW, CC, 8.5mm X 45mm; Item Number: TL1-10785045. 23. POLYAXIAL SCREW, CC, 8.5mm X 50mm; Item Number: TL1-10785050. 24. POLYAXIAL SCREW, CC, 8.5mm X 55mm; Item Number: TL1-10785055. 25. POLYAXIAL SCREW, CC, 8.5mm X 60mm; Item Number: TL1-10785060. — Reason: Polyaxial screws do not meet performance standards. — Status: Ongoing

    ›Sep 19, 2025device recall334d agoBeckman Coulter, Inc. device recall (Cls II)

    DxC 500i Clinical Analyzer Modules, DxC 500 AU Module w/ISE, DxC 500i (Part Number C63522), DxC 500 AU Module, DxC 500i (Part Number C63521), and Access 2 Module, DxC 500i (Part Number C13252) — Reason: Beckman Coulter has confirmed a software anomaly on DxI 9000 Access Immunoassay Analyzer and the DxC 500i Clinical Analyzer that may prevent correct application of user-specified manual dilution factors when ordering additional tests for samples already "In Progress" using the same "Sample ID number". This can lead to false low or high patient results and potential delays in reporting, risking erroneous diagnoses if undetected. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 19, 2025grant334d agoEMORY UNIVERSITY — SMILE (Sickle Cell Disease Microbiologic and Immunologic Links to Health)Emory University

    HL grant. $794,661. PI: Matthew Z Anderson

    full page →nih reporter ↗
    ›Sep 19, 2025grant334d agoUNIVERSITY OF HOUSTON — Mechanical and non-mechanical contributions to chronic neck, shoulder, arm, a...

    AR grant. $365,339. PI: Stacey Lynn Gorniak

    full page →nih reporter ↗
    ›Sep 19, 2025grant334d agoUNIVERSITY OF ARIZONA — Skeletal Maturity and Segmental Spinal Mobility Predict Successful Vertebral ...

    AR grant. $616,238. PI: Melanie Emily Boeyer

    full page →nih reporter ↗
    ›Sep 19, 2025grant334d agoUNIVERSITY OF WISCONSIN-MADISON — Re-evaluating the Duration in Children of TB Treatment (REDUCE TB): A Phase 2...

    AI grant. $164,241. PI: Anthony Joseph Garcia-Prats

    full page →nih reporter ↗
    ›Sep 19, 2025grant334d agoCINCINNATI CHILDRENS HOSP MED CTR — Improving Medication Adherence using an Adaptive mHealth Intervention in Adol...

    HL grant. $731,130. PI: Rachelle R. Ramsey

    full page →nih reporter ↗
    ›Sep 19, 2025grant334d agoBRIGHAM AND WOMEN'S HOSPITAL — Characterizing Biological Aging for Heart and Lung Diseases Using Multi-omics...Brigham and Women's Hospital

    HL grant. $177,120. PI: Yulu Chen

    full page →nih reporter ↗
    ›Sep 19, 2025grant334d agoGRADUATE SCHOOL OF PUBLIC HEALTH AND HEALTH POLICY — Streamlined Treatment and Evidence-based Adolescent counseling and Medication...

    MH grant. $1,057,586. PI: Philip Kreniske

    full page →nih reporter ↗
    ›Sep 19, 2025grant334d agoO2M TECHNOLOGIES, LLC — Advanced Imaging Methods in Pulse EPR

    CA grant. $1,164,814. PI: Boris Epel

    full page →nih reporter ↗
    ›Sep 19, 2025grant334d agoMASSACHUSETTS GENERAL HOSPITAL — Empowering cancer detection and monitoring with CampEx - CRISPR-accelerated m...Massachusetts General Hospital

    CA grant. $2,855,619. PI: Cesar M Castro

    full page →nih reporter ↗
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    full page →fda device recalls ↗
    $ANIP76.86+1.13%
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    $MDT92.64+2.25%
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    $TEM