16 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Stryker OrthoMap Precision Knee system
FDA 510(k)
FDA Class 2
·Neurology
Truline
FDA UDI
Arbill Industries, Inc.·00850052602406·Made in Malaysia. Black disposable nitrile. Siz...
Truline
FDA UDI
Arbill Industries, Inc.·10850052602120·
Bi-Metric® Revision Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868261305·
BI-METRIC REVISION HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304001138·
Novo Surgical Inc.
FDA UDI
NOVO SURGICAL, INC.·00842331179969·micro scissors, vannas-type cutting blades, 5.0...
BI-METRIC(R) HEAD/NECK PROVISIONAL
FDA UDI
Biomet Orthopedics, LLC·00880304307339·
VIPI BLOCK
FDA 510(k)
FDA Class 2
·Dental
MALE REMEEX SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OMNIPOD INSULIN PUMP
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·February 19, 2009
ATTAIN ABILITY PLUS
FDA Adverse Event
Injury
·MPRI·Product code OJX·October 10, 2014
GYNECARE GYNEMESH* PS
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTO·June 11, 2013
PFC SIGMA C/R POR FEM LF SZ3
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 7, 2011
AXOGUARD NERVE CONNECTOR AND PROTECTOR
FDA Adverse Event
Injury
·COOK BIOTECH·Product code JXI·October 24, 2019
RESTORE ADVANCED
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 25, 2016
MENTOR SILTEX ROUND MODERATE PROFILE
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·May 31, 2018