31 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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P.004 NC CARES TITANIUM AND CERAMIC ABUTMENTS
FDA 510(k)
FDA Class 2
·Dental
FIBONACCI™ PROXIMAL LATERAL TIBIA PLATE, LEFT, 5 HOLE
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665035193·
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481113697·LOCATOR R-Tx Abutment for iSy Connection Implan...
LOCATOR F-Tx
FDA UDI
Zest Anchors, LLC·00840481114670·LOCATOR F-Tx Abutment for iSy Connection Implan...
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR76000810051·Lingual cleat
FO NX Nail System
FDA UDI
FIELD ORTHOPAEDICS PTY LTD·09353903012559·0.8 Double-ended Trocar K-wire 100 mm 5/pkg
WAKO HDL-C/LDL-C CALIBRATOR
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PURE WATER SOLUTIONS CENTRAL WATER SYSTEM FOR HEMODIALYSIS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
9616026-2006-00240
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
9616026-2006-00244
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
9616026-2006-00239
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
9616026-2006-00222
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
9616026-2006-00252
FDA Adverse Event
Other
·Product code FII·June 21, 2006
9616026-2006-00245
FDA Adverse Event
Malfunction
·Product code FII·June 22, 2006
9616026-2006-00253
FDA Adverse Event
Other
·Product code FII·June 21, 2006
PRISMAFLEX SYSTEM
FDA Adverse Event
Malfunction
·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006
9616026-2006-00221
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006