10 results
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28ms
·
Sources: EU EUDAMED, US FDA
GUTTA PERCHA POINTS
FDA 510(k)
FDA Class 1
·Dental
MONDEAL
FDA UDI
MONDEAL Medical Systems GmbH·04050435061707·MCD Screw 3.0 x 14 mm M2
lockin...
Masel
FDA UDI
Ortho Organizers, Inc.·00190707034610·.014 Upper Value Brand Of Niti Natural Form Arc...
Lancer Gear
FDA UDI
LANCER ORTHODONTICS, INC.·00817573023820·CERVICAL"LANCER GEAR"BLACK/BLACK 5/PK
VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
PAINMASTER MCT PATCH
FDA 510(k)
FDA Class 2
·Neurology
OCUSCAN RXP
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOGY CTR·Product code IYO·May 1, 2014
ARTHROSCOPE
FDA Adverse Event
Injury
·MDT KYPHON SUNNYVALE MFG·Product code HRX·November 13, 2012
STERLING BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·September 10, 2010
Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026