10 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STAINLESS STEEL NONABSORBABLE SURGICAL SUTURE, USP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Polystar HK
FDA UDI
Merz Dental GmbH·D7091984151·anteriors; shade A3.5; mould D 68
P.F.C.
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295252412·P.F.C. TIBIAL INSERT FIXED BEARING CURVED 3 17....
Sklar®
FDA UDI
SKLAR CORPORATION·10649111312854·MILLESI MICRO SCISS CVD 6.25"
MODEL G7731D WASHER/DISINFECTOR FOR DENTAL INSTRU.
FDA 510(k)
FDA Class 2
·General Hospital
IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT
FDA 510(k)
FDA Class 2
·Dental
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 10, 2011
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code OYC·September 28, 2016
2.5MM X 25.4MM FLUTED ROUTER
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 18, 2013
Depuy P.F.C. Modular Knee System, curved tibial insert (CVD); polyethylene tibial insert, Sz 3, 17.5 mm; Ref 98-4151.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code JWH·May 26, 2005