22 results · 25ms · 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.

MEDRAD PHASED ARRAY 1.5T SHOULDER IMAGING SURFACE COIL

FDA 510(k)
FDA Class 2 ·Radiology

Lode B.V.

FDA UDI
Lode B.V.·08717524640033·960901 Corival rehab

P.F.C. SIGMA

FDA UDI
DEPUY (IRELAND)·10603295234470·P.F.C. SIGMA DISTAL AUGMENT SIZE 5 4mm RIGHT

VASHE WOUND CLEANSING SYSTEM

FDA 510(k)
FDA Unclassified ·Unknown

Xpert Carba-R

FDA 510(k)
FDA Class 2 ·Microbiology

TC3 RP TIBIAL INSERT S5,10.0

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·January 28, 2020

SIGMA FEM ADAPTER 5 DEGREE

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 28, 2020

MBT REVISION CEM TIB TRAY SZ 4

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·January 28, 2020

MBT TRAY SLEEVE POR M/L 37MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·January 28, 2020

UNIVERSAL FEM SLV FUL POR 40MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 28, 2020

PFC*SIGMA DIS AUG 4MM,SZ5,RGHT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 28, 2020

PFC SIGMA FEM POST AUG SZ5 8MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 28, 2020

PFC SIGMA FEM POST AUG SZ5 8MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 28, 2020

UNIVERSAL STEM 75X22MM FLUTED

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 28, 2020

UNIVERSAL STEM 75X18MM FLUTED

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 28, 2020

PFC*SIGMA TC3 FEM RT SZ5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 28, 2020

PFC*SIGMA DIS AUG 4MM,SZ5,RGHT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 28, 2020

SIGMA FEM ADAPTER NEUTRAL BOLT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·January 28, 2020

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 30, 2013

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWP·January 14, 2011