25 results · 23ms · 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.

MAMMOTOME EX

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNW·June 7, 2006

MAMMOTOME EX HAND HELD SYSTEM

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Baltic Denture System BDLoad

FDA UDI
Merz Dental GmbH·D7091033700·Baltic Denture System BDLoad BDLoad Mm7 PLSEbi...

JOBST Confidence

FDA UDI
BSN-Jobst GmbH·04059993469048·CONFIDENCE 1/KNEE HIGH/CLOSED TOE-FOOT FUNCTION...

JOBST Confidence

FDA UDI
BSN-Jobst GmbH·04059993474387·CONFIDENCE 3/KNEE HIGH/CLOSED TOE-FOOT FUNCTION...

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702248760·Elvarex 2/Thigh High/Closed Toe-Elephantiasis-V...

JOBST Confidence

FDA UDI
BSN-Jobst GmbH·04059993464104·CONFIDENCE 2/KNEE HIGH/CLOSED TOE-FOOT FUNCTION...

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702287066·ELVAREX 2/CHAP STYLE/OPEN TOE, KNEE FUNCTION/BLACK

SYNTHES HAMSTRING LOOP

FDA 510(k)
FDA Class 2 ·Orthopedic

ORTHOSIS HELMET MOLDING

FDA 510(k)
FDA Class 2 ·Neurology

ARCHITECT I1000SR ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·June 9, 2019

EXTENSION SET

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·April 3, 2013

TOTAL ASR ACET IMP SIZE 56

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD·Product code KWA·March 17, 2011

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·ANIMAS CORP.·Product code LZG·April 25, 2008

PINN CAN BONE SCREW 6.5MMX45MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code NDJ·December 1, 2014

ALTRX +4 10D 36IDX56OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·December 2, 2014

SROM STM STD 36+12L 13X18

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·December 2, 2014

PINN CAN BONE SCREW 6.5MMX25MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code NDJ·December 2, 2014

S-ROM*SLEEVE PRX ZTT, 18D-LRG

FDA Adverse Event
Injury ·DEPUY (IRELAND) 9616671·Product code LPH·December 2, 2014

ASPHERE M SPEC 11/13 36 +6

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 30, 2012