199 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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