Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) 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

BZR 2023-12-04

Maxtec MaxBlend2+p

Applicant Maxtec, LLC

K-Number K231895

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DRF 2023-12-02

Cosine-10TM Diagnostic Catheter

Applicant Medtronic, Inc.

K-Number K233397

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DYH 2023-12-01

AlignerFlow LC

Applicant Voco GmbH

K-Number K231817

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DWJ 2023-12-01

Medline ComfortTemp Patient Warming System

Applicant Medline Industries, LP

K-Number K231211

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ODC 2023-12-01

PENTAX Medical Gas/Water Feeding Valve OE-B14

Applicant Pentax of America, Inc.

K-Number K232249

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LJS 2023-12-01

CATHTONG III Tapered PICC Catheter

Applicant L&Z Us, Inc.

K-Number K233149

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NBW 2023-12-01

TRUENESS AIR Blood Glucose Monitoring System; TRUENESS Blood Glucose Monitoring System

Applicant Sinocare, Inc.

K-Number K231476

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LHI 2023-12-01

Vial2Bag Advanced® 13mm Admixture Device

Applicant West Pharma. Services IL, Ltd.

K-Number K230988

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QJP 2023-12-01

Slinky Catheter

Applicant Anoxia Medical, Inc.

K-Number K231179

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FOZ 2023-12-01

BD Nexiva Diffusics Closed IV Catheter System with BD MaxZero Needle-free Connector

Applicant Becton Dickinson Infusion Therapy Systems, Inc.

K-Number K233529

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ODP 2023-12-01

Align Cervical Interbody Fusion System

Applicant Acuity Surgical Devices, LLC

K-Number K230639

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DZE 2023-12-01

Single Platform SP1 Implant System

Applicant Southern Implants (Pty), Ltd.

K-Number K232418

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