8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BTL-899F
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GRAVITECH TM FLOW CONTROLLER PRIMARY SET/GRAVITECH FLOW CONTROLLER EXTENSION SET
FDA 510(k)
FDA Class 2
·General Hospital
POROUS MORPHIX SUTURE ANCHOR WITH FORCE FIBER SUTURE
FDA 510(k)
FDA Class 2
·Orthopedic
SILICONE ADVANCED OPTIC-VIOLET SHIELD
FDA Adverse Event
Malfunction
·BAUSCH & LOMB·Product code HQL·November 7, 2008
UNKNOWN DEPUY 50X32 LINER
FDA Adverse Event
Injury
·DEPUY WARSAW·Product code JDI·September 1, 2011
OBTRYX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 16, 2013
PULLUP
FDA Adverse Event
Malfunction
·S.B.M. SAS·Product code MBI·April 12, 2023
CODMAN Disposable Perforator, 14mm. Cranial perforator.
FDA Enforcement
Class I
·Ongoing·Integra LifeSciences Corp. (NeuroSciences)·May 14, 2025