8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
STAPLE REMOVER SR300P
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Stern Root Anchor® 5 Root Mini Refill Kit Ti
FDA UDI
STERNGOLD DENTAL LLC·00841549106729·The Stern Root AnchorSystem includes the Stern ...
END NIPPER CUTTER
FDA UDI
W.H. Holden, Inc.·D9288330850·
HEPAFIX BIOPSY NEEDLE SET
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PORTACLAMP
FDA 510(k)
FDA Class 2
·Cardiovascular
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 27, 2014
HALO90 ABLATION CATHETER
FDA Adverse Event
Other
·BARRX MEDICAL, INC.·Product code GEI·April 26, 2010
MEDPOR SURGICAL IMPLANT MATERIAL PREFORMED CRANIAL AND FACIAL IMPLAN
FDA Adverse Event
Injury
·STRYKER CRANIOMAXILLOFACIAL GEORGIA·Product code FWP·November 6, 2012