38 results
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39ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Pencylcap
FDA 510(k)
FDA Class 2
·General Hospital
Permacol
FDA UDI
SOFRADIM PRODUCTION·10884523000221·Surgical Implant
Epredia
FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693063753·The blades and knifes consumables are for use w...
TiMesh
FDA UDI
MEDTRONIC PS MEDICAL, INC.·00643169620407·ISOGRID 015-2050 STANDARD 75MM X 75MM
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741520500·
TiMesh®
FDA UDI
MEDTRONIC PS MEDICAL, INC.·00673978003214·ISOGRID 015-2050 STANDARD 75MM X 75MM
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100158·KRATZ-BARRAQUER SPECULUM LARGE
MORRISON MEDICAL
FDA UDI
MORRISON MEDICAL, LTD·00647921152052·PLAIN CARDBD SPLINT 24", CA 50
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674152050060·
Q-SWITCHED ND:YAG LASER SYSTEM, MODEL GLOBALCURE-SC6
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SOUNDSTAR ECO DIAGNOSTIC ULTRASOUND CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA UDI
Zimmer, Inc.·00889024033955·
Truliant
FDA UDI
Exactech, Inc.·10885862523341·PS NOTCH GUIDE, SIZE 5
TENDRIL STS
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. CRMD·Product code DTB·January 13, 2014
BIORAPTOR AB 2.9 MM
FDA Adverse Event
Malfunction
·SMITH & NEPHEW ENDOSCOPY·Product code HWC·July 7, 2011
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DXY·June 7, 2013
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 30, 2022
KYPHON BONE CEMENT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·April 23, 2019
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·March 18, 2026
METACROSS OTW PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 19, 2019