46 results · 26ms · Sources: EU EUDAMED, US FDA

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DISKOM

FDA 510(k)
FDA Class 2 ·Orthopedic

BI-METRIC X-SERIES HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304182646·

BI-METRIC X-SERIES HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304182943·

BI-METRIC X-SERIES HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304182349·

Tibial Trial Tray

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215062064·

Orthopedic Instruments

FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258699639·

12 LEAD GLOVE

FDA 510(k)
FDA Class 2 ·Cardiovascular

DERMA SCIENCES MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEY

FDA 510(k)
FDA Unclassified ·Unknown

REAMER SHAFT, MOD. TRINKLE BIXCUT 8.0 X 284 MM

FDA Adverse Event
Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·December 18, 2012

COCR CABLE/SLEEVE SET 2.0MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDQ·December 13, 2017

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 17, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011

PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code FTL·June 20, 2013

32MM M2A MOD HEAD STD NK

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 16, 2020

M2A-TAPER LINER SZ 41/32

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 16, 2020

M2A-T UNIV 2-HOLE SHL SZ 41/58

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 16, 2020

M2A-MAGNUM PF CUP 58OD/52ID

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·January 19, 2018

M2A-MAGNUM MOD HD SZ 52MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·January 19, 2018

BI-METRIC/X POR NC 15X155

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MEH·September 27, 2017

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·April 12, 2019