32 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PROSOFT
FDA 510(k)
FDA Class 2
·Dental
Z Liquid HT A4-S 100ml
FDA UDI
ARGEN CORPORATION, THE·D818121318·Dental porcelain/ceramic restoration kit
ZAVATION ROD CONNECTOR
FDA UDI
Zavation LLC·00197157016616·ROD CONNECTOR, PARALLEL SIDE LOADING/CLOSED 18m...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197040716·Super-Cut Reynolds Scissor
curved...
CLEARPATH 24
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
XIVE DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·June 20, 2016
BIA400 IMPLANT 4MM W ABUTMENT 8MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·April 28, 2016
BIA400 IMPLANT 4MM W ABUTMENT 12MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·October 11, 2016
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·June 26, 2016
BIA400 IMPLANT 4MM W ABUTMENT 8MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·May 25, 2016
BIA400 IMPLANT 4MM WITH ABUTMENT 12MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·June 6, 2016
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·July 21, 2016
BIA400 IMPLANT 4MM W ABUTMENT 12MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·January 13, 2016
BIA400 IMPLANT 4MM W ABUTMENT 10MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·October 5, 2015
ASKU
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·December 12, 2025
COCHLEAR BAHA ATTRACT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 14, 2016
BIA400 IMPLANT 4MM W ABUTMENT 8MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·March 18, 2016
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·September 22, 2014