24 results · 22ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

TBD

FDA 510(k)
FDA Class 2 ·Ophthalmic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526743670·ACHIMED ACHILLES SUPP SILVER IV

ATLANTIS® Anterior Cervical Plate System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994239938·SCREW 3120214 4.0 X 14 SELF TAP FIX

ATLANTIS® Anterior Cervical Plate System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000889319·SCREW 3120214 4.0 X 14 SELF TAP FIX

Unity Total Knee System

FDA UDI
CORIN LTD·05056139243530·UNITY KNEE™ PS-C INSERT - Size 2 x 14mm

Cortical Screw, Cannulated

FDA UDI
I.T.S. GmbH·09120069816143·Cortical Screw, Cannulated, D=2.0mm, L=14mm

CRYOPEN CRYOSURGICAL SYSTEM, K102214

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

APEX PS Knee

FDA UDI
Omni Life Science, Inc.·00841690113102·PS Insert, Size 2 x 14mm

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450191286·

General Instrument

FDA UDI
ALPHATEC SPINE, INC.·00840180513668·ALIF, Short Modular Rasped Rotating Distractor,...

CORNERSTONE PSR CERVICAL INTERBODY FUSION DEVICE

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDIAL ROTATION KNEE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDIAL ROTATION KNEE

FDA Adverse Event
Injury ·MATORTHO LIMITED·Product code JWH·January 22, 2016

MEDIAL ROATION KNEE

FDA Adverse Event
Malfunction ·MATORTHO LIMITED·Product code JWH·January 22, 2016

MEDIAL ROATION KNEE

FDA Adverse Event
Injury ·MATORHTO LIMITED·Product code JWH·January 22, 2016

MEDIAL ROTATION KNEE

FDA Adverse Event
Malfunction ·MATORTHO LIMITED·Product code JWH·January 22, 2016

MEDIAL ROTATION KNEE

FDA Adverse Event
Injury ·MATORTHO LIMITED·Product code JWH·January 22, 2016

REFORM PEDICLE SCREW SYSTEM

FDA Adverse Event
Injury ·PRECISION SPINE, INC·Product code HXX·December 18, 2024

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·Product code OYC·May 20, 2013

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·September 26, 2014