54 results · 23ms · Sources: EU EUDAMED, US FDA

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Powerpress Recovery Unit

FDA 510(k)
FDA Class 2 ·Physical Medicine

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772777617·LUMBAMED BASIC DORSAL STAY WM SILVER IV

LEONE SPA

FDA UDI
LEONE SPA·08033707061007·BRACKETS 22 MOL

SprintRay Standard Denture Base - Original Meharry

FDA UDI
Sprintray, Inc.·00850039704253·SprintRay Standard Denture Base is a light-cura...

24M - Southwest Gas Corp

FDA UDI
Certified Safety Manufacturing, Inc.·00766588010441·24M - Southwest Gas Corp

SURGISIS STAPLE LINE REINFORCEMENT

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

MAGNA FORTIS OPHTHALMOSCOPE DIAGNOSTIC KIT

FDA 510(k)
FDA Class 2 ·Ophthalmic

NOBELACTIVE TIULTRA NP 3.5X13MM

FDA Adverse Event
Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

NOBELACTIVE TIULTRA NP 3.5X13MM

FDA Adverse Event
Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

Trabecular Metal®

FDA UDI
Zimmer, Inc.·00889024118751·

Trabecular Metal®

FDA UDI
Zimmer, Inc.·00889024118768·

Trabecular Metal®

FDA UDI
Zimmer, Inc.·00889024118744·

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

PHYSIOMESH UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code FTL·April 22, 2021

PROCEED MESH

FDA Adverse Event
Injury ·ETHICON INC.·Product code FTL·April 22, 2021

BD SMARTSITE¿ VENTED VIAL ACCESS DEVICE, 20 MM

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code LHI·February 1, 2022

ENDURANT II STENT GRAFT

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·August 3, 2021

LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM WITH RAPIDPORT

FDA Adverse Event
Malfunction ·ALLERGAN·Product code LTI·June 27, 2013

JUVEDERM ULTRA PLUS

FDA Adverse Event
Injury ·ALLERGAN·Product code LMH·August 5, 2011

I-STAT 6+ CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE INC.·Product code MMI·September 23, 2008