10 results
·
24ms
·
Sources: EU EUDAMED, US FDA
TELEMETRY SYSTEM 315
FDA 510(k)
FDA Class 2
·Cardiovascular
CoRoent
FDA UDI
Nuvasive, Inc.·00887517360472·CoRoent SI Rasp, 8x17x14mm
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515204225·Flat Nose Pliers, 7" serrated and grooved
discovery®
FDA UDI
DENTAURUM GmbH & Co.KG·J011790144000·discovery® Bracket with hook, - 17° Torque, 0° ...
SERUM, HAPTOGLOBIN GOAT ANTI-HUMAN ACID
FDA 510(k)
FDA Class 2
·Immunology
MucoPEG
FDA 510(k)
FDA Unclassified
·Unknown
ITREL 3
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·May 5, 2014
EXTERNAL PULSE GENERATOR
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DTE·October 15, 2012
AUTOMATED PD SET W/CASSETTE4 PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 10, 2010
PROPONENT DR SL (Model L201)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025