8,286 results · 29ms · Sources: EU EUDAMED, US FDA

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MINI SHOPPER

FDA 510(k)
FDA Class 2 ·Physical Medicine

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033542798·

RIVIERA

FDA UDI
FGX INTERNATIONAL INC.·00887661636539·

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033542767·

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033542736·

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033542774·

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033542781·

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033542743·

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033542750·

MODIFICATION TO PROLITE PULSED LIGHT SYSTEM

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

Y2000 MANUAL RESUSCITATOR, MODEL RUGU01/RUG02 AND RUGH01/RUGH02

FDA 510(k)
FDA Class 2 ·Anesthesiology

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·March 20, 2013

TENDRIL STS

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011

LIFESHIELD

FDA Adverse Event
Other ·HOSPIRA INC·Product code FPA·March 14, 2008

IMPL TAPERED SCR-V HA 4.7 MM 4.5MM 11.5MM

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·April 26, 2024

IMPL TAPERED SCR-V SBM 3. 7MM 3.5MM 8MM

FDA Adverse Event
Malfunction ·ZIMMER DENTAL·Product code DZE·December 19, 2019

IMPL TAPERED SCR-V HA 3.7 MM 3.5MM 13MM

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·August 7, 2019

IMPL TAPERED SCR-V SBM 3.7MM 3.5MM 10MM

FDA Adverse Event
Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 29, 2026

IMPL TAPERED SCR-V SBM 3.7MM 3.5MM 10MM

FDA Adverse Event
Injury ·ZIMMER DENTAL·Product code DZE·February 23, 2022

IMPL TAPERED SCR-V SBM 3. 7MM 3.5MM 8MM

FDA Adverse Event
Malfunction ·ZIMMER DENTAL·Product code DZE·October 11, 2022