24 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LOOP/SQUARE ELECTRODE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
BASE
FDA UDI
Nuvasive, Inc.·00887517700926·BASE Ti HL Implant, 10x38x28mm 30°
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110980·STERILIZING CASE PLASTIC LARGE
Conveyor 900, TCA
FDA UDI
Thermo Fisher Scientific Oy·06438153000297·Conveyor 900, TCA is a module of TCAutomation L...
RGX 3 PEG SER A PATELLA 34MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HRY·December 23, 2019
iNSitu™ Hip System
FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127023842·Standard Screwdriver Bit T20
SURGEON'S GLOVE, POWDER FREE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Hisense 2MP/3MP LCD Monitor (HMD2C21/HMD3C21)
FDA 510(k)
FDA Class 2
·Radiology
Prolong® NexGen®
FDA UDI
Zimmer, Inc.·00889024207967·
Prolong® NexGen®
FDA UDI
Zimmer, Inc.·00889024207998·
Prolong® NexGen®
FDA UDI
Zimmer, Inc.·00889024263444·
Prolong® NexGen®
FDA UDI
Zimmer, Inc.·00889024263437·
Prolong® NexGen®
FDA UDI
Zimmer, Inc.·00889024208001·
Prolong® Highly Crosslinked Polyethylene
FDA UDI
Zimmer, Inc.·00889024670723·
Prolong® Highly Crosslinked Polyethylene
FDA UDI
Zimmer, Inc.·00889024670716·
Prolong® NexGen®
FDA UDI
Zimmer, Inc.·00889024207981·
Prolong® NexGen®
FDA UDI
Zimmer, Inc.·00889024207974·
NEXGEN STEMMED TIBIAL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·June 25, 2018
ADAPTA DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·February 9, 2013
MESH - COMPOSIX KUGEL
FDA Adverse Event
Injury
·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·July 16, 2014