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

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COMBAT READY CLAMP

FDA 510(k)
FDA Class 2 ·Cardiovascular

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772814688·GENUMEDI SILVER SIZE V

ACE

FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950019038·FORCEP IRIS TISSUE DELICATE 1X2 TEETH HALF CURV...

RHEAD

FDA UDI
Stryker GmbH·00886385025063·Recon Stem Implant 6mm Collar,Size 4

Mini Master Series

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746108563·DB BRACKET MINI MS MAX RIGHT CUSPID 022 TQ=+8 A...

The Brachiator Mini External Fixation System

FDA UDI
Paragon 28, Inc.·00889795151919·Half Pin, Ø2.0 x 100mm OAL x 25mm THD

Pulmoguard

FDA UDI
S D I DIAGNOSTICS INC·B279S293102025·Pulmonary function test filter

RIGID GAS PERMEABLE CONTACT LENS

FDA 510(k)
FDA Class 2 ·Ophthalmic

MACROPORE SURGIWRAP (TS)

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

RHEAD RECON STEM IMPLANT NON-COATED, SIZE 4

FDA Adverse Event
Malfunction ·STRYKER GMBH·Product code KWI·December 29, 2015

Widex

FDA UDI
Widex A/S·05706069425000·Widex MENU ME-X ITE (Light beige ) Telecoil, Vo...

LEAD MODEL UNKNOWN

FDA Adverse Event
Injury ·LIVANOVA USA, INC.·Product code LYJ·February 7, 2025

OCTRODE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 6, 2013

HUDSON INCENTIVE SPIROMETER

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code BWF·April 13, 2011

ENDOVIVE STANDARD PEG KITS PULL METHOD

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNT·August 7, 2008

MOSAIC MITRAL BIOPROSTHETIC VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·October 25, 2025

PHENOM

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·March 6, 2025

REBAR

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·March 6, 2025

TOTAL KNEE PACK

FDA Adverse Event
Malfunction ·DEROYAL INDUSTRIES, INC.·Product code LRO·February 19, 2025

rHead Recon Stem Implant 6mm Collar, Size 4. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.

FDA Enforcement
Class II ·Terminated·Howmedica Osteonics Corp.·August 15, 2018