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calendar

34 catalysts · 11 approval · 10 device 510k · 10 device recall · 3 device pma

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no tagged catalysts yet

Week of Oct 27, 2025

34
›
Oct 27, 2025
approval
306d ago
TRAMADOL HYDROCHLORIDE — FDA approvalTrigen Laboratories Inc

Sponsor: PLIVA. Form: TABLET. Route: ORAL

full page →fda approvals ↗
›Oct 27, 2025approval306d agoOPDIVO QVANTIG (NIVOLUMAB) — FDA approval(hyaluronidase (recombinant, human) + nivolumab)

Sponsor: BRISTOL-MYERS SQUIBB. Form: INJECTABLE. Route: SUBCUTANEOUS

full page →(hyaluronidase (recombinant, human) + nivolumab) →fda approvals ↗
›Oct 27, 2025approval306d agoOPDIVO QVANTIG (NIVOLUMAB) — FDA approval(hyaluronidase (recombinant, human) + nivolumab)

Sponsor: BRISTOL-MYERS SQUIBB. Form: INJECTABLE. Route: SUBCUTANEOUS

full page →(hyaluronidase (recombinant, human) + nivolumab) →fda approvals ↗
›Oct 27, 2025approval306d agoLOMUSTINE — FDA approvalLOMUSTINE

Sponsor: CARNEGIE. Form: CAPSULE. Route: ORAL

full page →LOMUSTINE →fda approvals ↗
›Oct 27, 2025approval306d agoGLYCOPYRROLATE — FDA approvalFresenius Kabi USA LLC

Sponsor: AJENAT PHARMS. Form: SOLUTION. Route: ORAL

full page →fda approvals ↗
›Oct 27, 2025approval306d agoCOLUMVI (GLOFITAMAB-GXBM) — FDA approvalglofitamab

Sponsor: GENENTECH INC. Form: INJECTABLE. Route: INJECTION

full page →glofitamab →fda approvals ↗
›Oct 27, 2025approval306d agoDUREZOL (DIFLUPREDNATE) — FDA approvalDIFLUPREDNATE

Sponsor: SANDOZ. Form: EMULSION. Route: OPHTHALMIC

full page →DIFLUPREDNATE →fda approvals ↗
›Oct 27, 2025approval306d agoPOTASSIUM CHLORIDE — FDA approvalTWi Pharmaceuticals Inc

Sponsor: TWI PHARMS. Form: TABLET, EXTENDED RELEASE. Route: ORAL

full page →fda approvals ↗
›Oct 27, 2025approval306d agoSEVELAMER CARBONATE — FDA approvalRenvela

Sponsor: NAVINTA LLC. Form: TABLET. Route: ORAL

full page →Renvela →fda approvals ↗
›Oct 27, 2025approval306d agoASTEPRO ALLERGY (AZELASTINE HYDROCHLORIDE) — FDA approvalWallace Pharmaceuticals Inc

Sponsor: BAYER HLTHCARE. Form: SPRAY, METERED. Route: NASAL

full page →fda approvals ↗
›Oct 27, 2025approval306d agoKINERET (ANAKINRA) — FDA approvalSobi Inc

Sponsor: BIOVITRUM AB. Form: VIAL. Route: SUBCUTANEOUS

full page →fda approvals ↗
›Oct 27, 2025device 510k306d agoCircle Cardiovascular Imaging, Inc. — cvi42 Coronary Plaque Software Application (510k cleared)

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

full page →fda device 510k ↗
›Oct 27, 2025device 510k306d agoPatriot Laser, LLC — Patriot Duo (510k cleared)

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

full page →fda device 510k ↗
›Oct 27, 2025device 510k306d agoShenzhen Jamr Technology Co., Ltd. — Blood Pressure Monitor (B73, BE23T) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

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

full page →fda device 510k ↗
›Oct 27, 2025device 510k306d agoOsteocentric Technologies, Inc. — OsteoCentric Navigated Instruments System (510k cleared)

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

full page →fda device 510k ↗
›Oct 27, 2025device 510k306d agoTouchbeauty Beauty & Health ( Shenzhen ) Co., Ltd — VITA Multi-Function Head Brush (TB-2443F, TB-2442AF, TB-2343F, TB-2442F) (510k cleared)

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

full page →fda device 510k ↗
›Oct 27, 2025device 510k306d agoTechfit Digital Surgery, Inc. — TECHFIT Patient-Specific Cranial System (510k cleared)

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

full page →fda device 510k ↗
›Oct 27, 2025device 510k306d agoFimilla (Shanghai) Maternity & Baby Articles Co., Ltd. — Electric Breast Pump (HL-3058, F5112) (510k cleared)

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

full page →fda device 510k ↗
›Oct 27, 2025device 510k306d agoViet Phu Trade and Import Export Co., Ltd. — Disposable Vinyl Examination Gloves (510k cleared)

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

full page →fda device 510k ↗
›Oct 27, 2025device 510k306d agoAffinity Biosensors, LLC — LifeScale Gram Negative Kit (LSGN) with the LifeScale AST system (510k cleared)

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

full page →fda device 510k ↗
›Oct 27, 2025device 510k306d agoFimilla (Shanghai) Maternity & Baby Articles Co., Ltd. — Electric Breast Pump (HL-3060, F5113) (510k cleared)

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

full page →fda device 510k ↗
›Oct 27, 2025device pma306d agoW. L. Gore & Associates, Inc. — GORE® VIATORR® TIPS Endoprosthesis with Controlled Expansion (PMA supplement)

Supplement type: Normal 180 Day Track. Product code: MIR. Advisory committee: CV. Decision: APPR

full page →fda device pma ↗
›Oct 27, 2025device pma306d agoBoston Scientific Corp — ROTAPRO™ Rotational Atherectomy System (PMA supplement)BOSTON SCIENTIFIC CORP

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

full page →fda device pma ↗
›Oct 27, 2025device pma306d agoEdwards Lifesciences, LLC — TRIFORMIS RESILIA Tricuspid Valve (PMA supplement)Edwards Lifesciences Corp

Supplement type: Panel Track. Product code: LWR. Advisory committee: CV. Decision: APPR

full page →fda device pma ↗
›Oct 27, 2025device recall306d agoMedline Industries, LP device recall (Cls II)

Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25660QS — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

full page →fda device recalls ↗
›Oct 27, 2025device recall306d agoMedline Industries, LP device recall (Cls II)

Quick Strip Fabric Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25650QS — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

full page →fda device recalls ↗
›Oct 27, 2025device recall306d agoMedline Industries, LP device recall (Cls II)

Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

full page →fda device recalls ↗
›Oct 27, 2025device recall306d agoMedline Industries, LP device recall (Cls II)

Fur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON256133QS — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

full page →fda device recalls ↗
›Oct 27, 2025device recall306d agoPhilips North America device recall (Cls II)

Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL FLUOROSCOPIC XRAY SYSTEM — Reason: Between July 2024 and June 2025, Philips Azurion R3.0 systems with a FlexArm stand were shipped without the Source-to-Skin Distance (SSD) Spacer. The SSD spacer is necessary to meet the FDA minimum source-skin distance requirement of 38 cm for standard fluoroscopy applications. — Status: Ongoing

full page →fda device recalls ↗
›Oct 27, 2025device recall306d agoMedline Industries, LP device recall (Cls II)

CURAD Germ-Shield Touch-Free Fabric Bandages, Sterile, 0.75" x 3", 30/Box, Medline Item Number CUR1930F — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

full page →fda device recalls ↗
›Oct 27, 2025device recall306d agoMedline Industries, LP device recall (Cls II)

Curad Quick Strip Fabric Bandages Containing 30 Bandages of 3/4" x 3", Medline Item Number CUR1930P — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

full page →fda device recalls ↗
›Oct 27, 2025device recall306d agoMedline Industries, LP device recall (Cls II)

MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C — Reason: Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of their Luer Tip Caps after confirming through internal testing that certain BD Luer Tip Cap trays failed routine biocompatibility testing. Although the tip cap covers a small surface area of the syringe and does not come in direct contact with patients, there is the potential that the failure of a biocompatibility test may have varying consequences ranging from no harm or clinical impact to potential for sensitization, irritation, pyrogenicity, acute systemic toxicity or hemolysis depending on the nature and duration of contact with the syringe. — Status: Ongoing

full page →fda device recalls ↗
›Oct 27, 2025device recall306d agoNipro Medical Corporation device recall (Cls II)

Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only — Reason: Screw may loosen or fallout of Hemodialysis system — Status: Ongoing

full page →fda device recalls ↗
›Oct 27, 2025device recall306d agoMedline Industries, LP device recall (Cls II)

Quick Strip Plastic Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25600QS — Reason: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product. — Status: Ongoing

full page →fda device recalls ↗
$EW91.33-2.47%
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$BMY67.25-0.48%
$FRTRY
$BMY67.25-0.48%