16 results · 21ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

7000 SERIES MODULAR TIBIAL COMPONENTS

FDA 510(k)
FDA Class 2 ·Orthopedic

DIASTAT ANTI-SM/RNP

FDA 510(k)
FDA Class 2 ·Immunology

AUTO SUTURE ENDOSCOPIC TA SURGICAL STAPLER

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

PERFORMANCE MODULAR TIBIAL TRAY SML

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

E1 HI-WALL LINER RINGLOC-X 60MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·January 10, 2017

PERFORMANCE FEMORAL STEM 16X100MM

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

POLISHED IBEAM TIB TRAY 71MM

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·July 11, 2016

NON-POROUS PERF TIB TRAY-XSML

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·March 23, 2018

POLISHED FINNED TIBIAL TRAY 71 MM

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·March 10, 2017

POLISHED FINNED 1 PIECE TIBIAL TRAY

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 12, 2017

POLISHED FINNED TIBIAL TRAY 75MM

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·July 10, 2017

PRIM SYM SET 2 CL

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·May 16, 2014

POWER PRO AMBULANCE COT

FDA Adverse Event
Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code INK·November 16, 2010

ASR ACETABULAR IMPLANT 50

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·January 15, 2013

MAXIM PRIMARY FEMORAL COMPONENT 75 MM LEFT / POROUS 75 LT

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 30, 2017

DCM MAXIM PRIMARY TIBIAL BEARING 12 MM THICK X 71/75 WIDE ARCOM UHMWPE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 30, 2017