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

MAX 2019-01-07

TiWAVE-L Porous Titanium Lumbar Cage

Applicant Kalitec Medical, LLC

K-Number K182210

View Details →

JEY 2019-01-07

Stryker Facial iD Plating System

Applicant Stryker

K-Number K182305

View Details →

HRX 2019-01-07

Precision Ideal Eyes Arthroscopes

Applicant Stryker

K-Number K183470

View Details →

MAX 2019-01-07

FlareHawk Interbody Fusion System

Applicant Integrity Implants, Inc.

K-Number K182114

View Details →

NHA 2019-01-07

Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases

Applicant Medentika GmbH

K-Number K180564

View Details →

KIF 2019-01-04

BIO-C TEMP

Applicant Angelus Industria DE Produtos Odontologicos S/A

K-Number K180199

View Details →

HIH 2019-01-04

Polygon Resection Device

Applicant Polygon Medical, Inc.

K-Number K182675

View Details →

MQK 2019-01-04

Rapid-i™ Kit

Applicant Vitrolife Sweden AB

K-Number K181461

View Details →

EOQ 2019-01-04

GlideScope BFlex Single-Use Bronchoscope System

Applicant Verathon Medical (Canada) Ulc

K-Number K183256

View Details →

MBI 2019-01-04

CrossFT Knotless Deep Thread Suture Anchor with Disposable Driver

Applicant Conmed Corporation

K-Number K182621

View Details →

DZE 2019-01-04

Straumann PURE Ceramic Implant System

Applicant Institut Straumann AG

K-Number K180477

View Details →

JOJ 2019-01-04

Celerity HP Chemical Indicator (CI)

Applicant Steris Corporations

K-Number K183295

View Details →

Page 1975 of 2738

↑