9 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SEMPERMED SURGEONS' GLOVES - SUPREME
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
AXSOS
FDA UDI
Stryker GmbH·07613154489831·X-Ray Template Compression Plate
Polystar Selection EDITION
FDA UDI
Merz Dental GmbH·D7091981096·anteriors; shade A3.5; mould BIS2
Avenue P Cage System
FDA 510(k)
FDA Class 2
·Orthopedic
HEARING AID, EYEGLASS, B-12
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
ASR ACETABULAR IMPLANT 54
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·February 27, 2013
SENSIA DR
FDA Adverse Event
Death
·MEDTRONIC MED REL, INC.·Product code NVZ·February 8, 2011
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·UNKNOWN·Product code ITI·August 5, 2014
Angiotech Pediatric Bone Marrow Needle. Pediatric Bone Marrow Needle. STERILE. Product Number: ION18015. 510k K980196. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended Use: Pediatric Bone Marrow Needle
FDA Recall
Terminated
·Medical Device Technologies, Inc.·Product code KNW·September 1, 2009