Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

MBI 2026-07-09

Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one black knotless and one blue MINITAPE suture (72205981); Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one blue knotless and one black MINITAPE suture (72205982)

Applicant Smith & Nephew, Inc.

K-Number K261968

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QJP 2026-07-09

Millipede88 Access Catheter

Applicant Perfuze, Ltd.

K-Number K253901

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ODP 2026-07-08

C.A. Medical Interbody Fusion System

Applicant C.A. Medical, LLC

K-Number K254130

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HRS 2026-07-08

Alians Elbow S

Applicant Newclip Technics

K-Number K261191

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QFM 2026-07-08

CXRDetectAI

Applicant Neurocareai, Inc. (Dba Savelife.Ai)

K-Number K253751

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MUJ 2026-07-08

Virtual Cone (1.0)

Applicant Varian Medical Systems, Inc.

K-Number K260750

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SAN 2026-07-08

VITEK REVEAL GN AST Assay and VITEK REVEAL AST System

Applicant bioMerieux, Inc.

K-Number K260160

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DPW 2026-07-08

BlueDop Vascular Expert

Applicant BlueDop Medical, Ltd.

K-Number K260700

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EBI 2026-07-08

Denture Base Resin V2

Applicant Formlabs Ohio, Inc.

K-Number K262300

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DWJ 2026-07-08

ThermAffyx(TM) Patient Safety System

Applicant Stihler Electronic GmbH

K-Number K260278

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ITI 2026-07-08

Electric Wheelchair

Applicant Ningbo Resshidi Medical Devices Co., Ltd.

K-Number K261396

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QEP 2026-07-08

cobas CT/NG for use on the cobas 5800/6800/8800 systems; cobas TV/MG for use on the cobas 5800/6800/8800 systems

Applicant Roche Molecular Systems, Inc.

K-Number K260917

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