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calendar

46 catalysts · 15 device 510k · 15 device recall · 11 device pma · 5 approval

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2026-08-10: 0 catalysts2026-08-11: 16 catalysts2026-08-12: 19 catalysts2026-08-13: 19 catalysts2026-08-14: 4 catalysts2026-08-15: 0 catalysts2026-08-16: 0 catalysts2026-08-17: 1 catalyst2026-08-18: 2 catalysts2026-08-19: 2 catalysts2026-08-20: 0 catalysts2026-08-21: 0 catalysts2026-08-22: 0 catalysts2026-08-23: 0 catalysts2026-08-24: 0 catalysts2026-08-25: 0 catalysts2026-08-26: 1 catalyst2026-08-27: 1 catalyst2026-08-28: 0 catalysts2026-08-29: 0 catalysts2026-08-30: 0 catalysts2026-08-31: 0 catalysts2026-09-01: 1 catalyst2026-09-02: 0 catalysts2026-09-03: 1 catalyst2026-09-04: 0 catalysts2026-09-05: 0 catalysts2026-09-06: 0 catalysts2026-09-07: 0 catalysts2026-09-08: 0 catalysts2026-09-09: 0 catalysts2026-09-10: 0 catalysts2026-09-11: 0 catalysts2026-09-12: 0 catalysts2026-09-13: 0 catalysts2026-09-14: 0 catalysts2026-09-15: 0 catalysts2026-09-16: 0 catalysts2026-09-17: 0 catalysts2026-09-18: 0 catalysts2026-09-19: 0 catalysts2026-09-20: 0 catalysts2026-09-21: 0 catalysts2026-09-22: 0 catalysts2026-09-23: 2 catalysts2026-09-24: 0 catalysts2026-09-25: 0 catalysts2026-09-26: 0 catalysts2026-09-27: 0 catalysts2026-09-28: 0 catalysts2026-09-29: 0 catalysts2026-09-30: 0 catalysts2026-10-01: 0 catalysts2026-10-02: 0 catalysts2026-10-03: 0 catalysts2026-10-04: 0 catalysts2026-10-05: 0 catalysts2026-10-06: 0 catalysts2026-10-07: 0 catalysts2026-10-08: 2 catalysts2026-10-09: 0 catalysts2026-10-10: 0 catalysts2026-10-11: 0 catalysts2026-10-12: 0 catalysts2026-10-13: 1 catalyst2026-10-14: 1 catalyst2026-10-15: 0 catalysts2026-10-16: 0 catalysts2026-10-17: 0 catalysts2026-10-18: 0 catalysts2026-10-19: 1 catalyst2026-10-20: 2 catalysts2026-10-21: 2 catalysts2026-10-22: 2 catalysts2026-10-23: 1 catalyst2026-10-24: 0 catalysts2026-10-25: 0 catalysts2026-10-26: 1 catalyst2026-10-27: 8 catalysts2026-10-28: 12 catalysts2026-10-29: 21 catalysts2026-10-30: 4 catalysts2026-10-31: 0 catalysts2026-11-01: 0 catalysts2026-11-02: 8 catalysts2026-11-03: 17 catalysts2026-11-04: 22 catalysts2026-11-05: 36 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts
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no tagged catalysts yet

Week of Aug 4, 2025

46
›
Aug 8, 2025
approval
368d ago
SODIUM ACETATE — FDA approvalSODIUM ACETATE

Sponsor: AMNEAL. Form: SOLUTION. Route: INTRAVENOUS

full page →SODIUM ACETATE →fda approvals ↗
›Aug 8, 2025approval368d agoHERNEXEOS (ZONGERTINIB) — FDA approvalzongertinib

Sponsor: BOEHRINGER INGELHEIM. Form: TABLET. Route: ORAL

full page →zongertinib →fda approvals ↗
›Aug 8, 2025approval368d agoACTEMRA (TOCILIZUMAB) — FDA approvaltocilizumab

Sponsor: GENENTECH. Form: INJECTABLE. Route: INJECTION

full page →tocilizumab →fda approvals ↗
›Aug 8, 2025approval368d agoACTEMRA (TOCILIZUMAB) — FDA approvaltocilizumab

Sponsor: GENENTECH. Form: INJECTABLE. Route: INTRAVENOUS, SUBCUTANEOUS

full page →tocilizumab →fda approvals ↗
›Aug 8, 2025approval368d agoIRON SUCROSE — FDA approvalsuccharated ferric oxide

Sponsor: SANDOZ. Form: INJECTABLE. Route: INTRAVENOUS

full page →succharated ferric oxide →fda approvals ↗
›Aug 8, 2025device pma368d agoBoston Scientific Corp — Eluvia™ Drug-Eluting Vascular Stent System (PMA supplement)BOSTON SCIENTIFIC CORP

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

full page →fda device pma ↗
›Aug 8, 2025device pma368d agoABBOTT MEDICAL — Esprit™ BTK Everolimus Eluting Resorbable Scaffold System (PMA supplement)Postsurgical Therapeutics Inc

Supplement type: Normal 180 Day Track No User Fee. Product code: NXW. Advisory committee: CV. Decision: APPR

full page →fda device pma ↗
›Aug 8, 2025device pma368d agoAbiomed, Inc. — Impella CP with SmartAssist System (PMA supplement)Abion Inc

Supplement type: 135 Review Track For 30-Day Notice. Product code: OZD. Advisory committee: CV. Decision: APPR

full page →fda device pma ↗
›Aug 8, 2025device pma368d agoNyxoah S.A. — Genio® System 2.1 (PMA)Nyxoah SA

Product code: MNQ. Advisory committee: AN. Decision: APPR

full page →fda device pma ↗
›Aug 8, 2025device pma368d agoMentor Corp. — MENTOR™ MemoryGel™ Silicone Gel-Filled Breast Implants (PMA supplement)

Supplement type: 30-Day Notice. Product code: FTR. Advisory committee: SU. Decision: OK30

full page →fda device pma ↗
›Aug 8, 2025device pma368d agoAbbott Molecular, Inc. — Vysis CLL Fish Probe Kit (PMA supplement)

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

full page →fda device pma ↗
›Aug 8, 2025device pma368d agoMentor Worldwide, LLC — MENTOR™ Saline-Filled and SPECTRUM™ Breast Implants (PMA supplement)Revalesio Corp

Supplement type: 30-Day Notice. Product code: FWM. Advisory committee: SU. Decision: OK30

full page →fda device pma ↗
›Aug 8, 2025device pma368d agoLife Technologies Corporation — Oncomine Dx Target Test (PMA supplement)

Supplement type: Normal 180 Day Track. Product code: PQP. Advisory committee: PA. Decision: APPR

full page →fda device pma ↗
›Aug 8, 2025device pma368d agoBoston Scientific Corporation — lnnova™ Vascular Self Expanding Stent (PMA supplement)BOSTON SCIENTIFIC CORP

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

full page →fda device pma ↗
›Aug 8, 2025device pma368d agoMentor Worldwide, LLC — MENTOR™ MemoryShape™ Breast Implants (PMA supplement)

Supplement type: 30-Day Notice. Product code: FTR. Advisory committee: SU. Decision: OK30

full page →fda device pma ↗
›Aug 8, 2025device pma368d agoBoston Scientific Corp — Epic™ Vascular Self-Expanding Stent System (PMA supplement)BOSTON SCIENTIFIC CORP

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

full page →fda device pma ↗
›Aug 8, 2025device recall368d agoBaxter Healthcare Corporation device recall (Cls II)Baxter Healthcare Corp

Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8 m), Product Code REF 2C8519; intravascular administration set — Reason: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoRAYSEARCH LABORATORIES AB device recall (Cls II)

RayStation with the following product descriptions: 1. RayStation 11B, Software Version: 12.0.0.932. 2. RayStation 11B Service Pack 1, Software Version: 12.1.0.1221. 3. RayStation 11B Service Pack 2, Software Version: 12.0.3.68. 4. RayStation 11B Service Pack 3, Software Version: 12.0.4.12. 5. RayStation 11B Service Pack Toshiba 1, Software Version: 12.3.0.119. Product Description: Radiation Therapy Treatment Planning System. — Reason: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoRAYSEARCH LABORATORIES AB device recall (Cls II)

RayStation with the following product descriptions: 1. RayStation 8B, Software Version: 8.1.0.47. 2. RayStation 8B Service Pack 1, Software Version: 8.1.1.8. 3. RayStation 8B Service Pack 2, Software Version: 8.1.2.5. 4. RayStation 9A, Software Version: 9.0.0.113. 5. RayStation 9A Service Pack 1, Software Version: 9.0.1.142. Product Description: Radiation Therapy Treatment Planning System. — Reason: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoPhilips Medical Systems Nederland B.V. device recall (Cls II)

IntelliSpace Cardiovascular, Software 8.0.0.4. — Reason: Software issue that results in the display of outdated information. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoSchiller, Ag device recall (Cls II)

Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006 — Reason: Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoMedline Industries, LP device recall (Cls I)

Sterile Medline Convenience Kits: 1) EXTREMITY PACK, Model Number: DYNJ45701B — Reason: Convenience kits labeled as sterile have not gone through the sterilization process. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoRAYSEARCH LABORATORIES AB device recall (Cls II)

RayStation with the following product descriptions: 1. RayStation 11A, Software Version: 11.0.0.951. 2. RayStation 11A Service Pack 1, Software Version: 11.0.1.29. 3. RayStation 11A Service Pack 2, Software Version: 11.0.3.116. 4. RayStation 11A Service Pack 3, Software Version: 11.0.4.15. Product Description: Radiation Therapy Treatment Planning System. — Reason: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoRAYSEARCH LABORATORIES AB device recall (Cls II)

RayStation with the following product descriptions: 1. RayStation 9B, Software Version: 9.1.0.933. 2. RayStation 9B Service Pack 1, Software Version: 9.2.0.483. 3. RayStation 10A, Software Version: 10.0.0.1154. 4. RayStation 10A Service Pack 1, Software Version: 10.0.1.52. 5. RayStation 10A Service Pack 2, Software Version: 10.0.2.10. Product Description: Radiation Therapy Treatment Planning System. — Reason: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoRAYSEARCH LABORATORIES AB device recall (Cls II)

RayStation with the following product descriptions: 1. RayStation 6 Service Pack 1, Software Version: 6.1.1.2. 2. RayStation 6 Service Pack 2, Software Version: 6.2.0.7. 3. RayStation 6 Service Pack 3, Software Version: 6.3.0.6. Product Description: Radiation Therapy Treatment Planning System. — Reason: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoMedline Industries, LP device recall (Cls I)

Sterile Medline Convenience Kits: 1) MAJOR PACK L-F, Model Number: DYNJ0382730O; 2) LB BASIC CUSTOM PACK, Model Number: DYNJ61038B — Reason: Convenience kits labeled as sterile have not gone through the sterilization process. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoRAYSEARCH LABORATORIES AB device recall (Cls II)

RayStation with the following product descriptions: 1. RayStation 10B, Software Version: 10.1.0.613. 2. RayStation 10B Service Pack 1, Software Version: 10.1.1.54. Product Description: Radiation Therapy Treatment Planning System. — Reason: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoRAYSEARCH LABORATORIES AB device recall (Cls II)

RayStation with the following product descriptions: 1. RayStation 12A, Software Version: 13.0.0.1547. 2. RayStation 12A Service Pack 1, Software Version: 13.1.0.144. 3. RayStation 12A Service Pack 2, Software Version: 13.1.1.89. Product Description: Radiation Therapy Treatment Planning System. — Reason: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoGreiner Bio-One North America, Inc. device recall (Cls II)

Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2%, REF: 454322 — Reason: Blood collection tubes were manufactured with the label applied too high on the tube, which shifted the printed fill level mark upward, which could result in unnecessary sample rejection and repeat collections. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoRAYSEARCH LABORATORIES AB device recall (Cls II)

RayStation with the following product descriptions: 1. RayStation 7, Software Version: 7.0.0.19. 2. RayStation 8A, Software Version: 8.0.0.61. 3. RayStation 8A Service Pack 1, Software Version: 8.0.1.10. Product Description: Radiation Therapy Treatment Planning System. — Reason: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device recall368d agoRAYSEARCH LABORATORIES AB device recall (Cls II)

RayStation with the following product descriptions: 1. RayStation 2023B, Software Version: 14.0.0.3338. 2. RayStation 2024A, Software Version: 15.0.0.430. 3. RayStation 2024A SP3, Software Version: 15.1.3.10. Product Description: Radiation Therapy Treatment Planning System. — Reason: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique. — Status: Ongoing

full page →fda device recalls ↗
›Aug 8, 2025device 510k368d agoVive Health, LLC — Coretech Compression System (Coretech RHB3003) (510k cleared)

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoAqua Medical, Inc. — Aqua Medical RF Vapor Ablation System (510k cleared)AVITA Medical, Inc.

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoParkell, Inc. — Parkell Pit and Fissure Sealant (510k cleared)

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoIntegra Lifesciences Production Corporation — Codman Libertís Shunt Catheter with Bactiseal and Endexo Technology (510k cleared)

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoEmblation Limited — swiftPro System (SWF-SPS); Swift System (SWF-SYS) (510k cleared)

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoElevation Spine — SABER-C System (510k cleared)

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoGuangzhou Red Pine Medical Instrument Co., Ltd. — Single-Use Video Flexible Cysto-Nephroscope (RP-U-C01F, RP-U-C01FS) (510k cleared)

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoGlobal Protection Corp. — Plain Water-based Lubricant (510k cleared)

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoCarl Zeiss Meditec Cataract Technology, Inc. — MICOR 700 with Auto I/A (510k cleared)

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoTonica Elektronik A/S — MagVenture TMS Therapy System (510k cleared)

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoBecton, Dickinson and Company — BD Phoenix Automated Microbiology System - GN Eravacycline (0.125-2 µg/mL) (510k cleared)BECTON DICKINSON & CO

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoGlobal Protection Corp. — Water-based Lubricant (510k cleared)

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoAmdt Holdings, Inc. — SixFix™ Hexapod Fixator and Deformity Analysis and Correction Software (DACS) (510k cleared)AMAZE HOLDINGS, INC.

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoHebei Newangie Technology Co., Ltd. — Diode laser device (BM091) (510k cleared)

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

full page →fda device 510k ↗
›Aug 8, 2025device 510k368d agoMr Surgical Solutions, LLC — OptiVu™ Shoulder (510k cleared)

Product code: SBF. Advisory committee: Neurology. Type: Special

full page →fda device 510k ↗
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$BSX50.46+2.33%
$BSX50.46+2.33%
$AMZE
$RCEL7.6000-2.19%
$BSX50.46+2.33%
$NYXH
$BDX179.63+1.57%