25 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRIMEWIRE PRESTIAGE PRESSURE GUIDE WIRE, MODELS 8185, 8185J, 8300, 8300J
FDA 510(k)
FDA Class 2
·Cardiovascular
Premier
FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·00856402006238·Decan Stopper Size 8 Closure 3/4
AIM™FEMORAL NAIL
FDA UDI
Biomet Orthopedics, LLC·00887868003073·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16711009300·
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·04546540133748·PERIOST. ELEVATOR, HENDERSON, SHARP
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776410636·Henderson Periosteal Elevator D/E 5.5/10mm Shar...
LEONE SPA
FDA UDI
LEONE SPA·08033707002819·COIL SPRINGS MEMORIA 030/009 OPEN
Mariner MIS
FDA UDI
Seaspine Orthopedics Corporation·10889981294984·Stylet Shuttle, 30mm
Life Instruments
FDA UDI
Life Instrument Corporation·M930810093010·Brun Curette #3/0 Ang
Life Instruments
FDA UDI
Life Instrument Corporation·M93081009302C0·Brun Curette #3/0 rev angle flatback
Treatment Pack, 50 Pack
FDA UDI
NEURONETICS, INC.·10850005944239·Treatment Pack to be used with the SenStar Conn...
Life Instruments
FDA UDI
Life Instrument Corporation·M930810093020·Brun Curette #3/0 Rev Ang
Life Instruments
FDA UDI
Life Instrument Corporation·M930810093000·Brun Curette #3/0 Str
LIFT VB SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
GATIFLOXACIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC
FDA 510(k)
FDA Class 2
·Microbiology
BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·May 15, 2018
GYNECARE TVT-ABBREVO MINI LCM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·November 30, 2021
NEOPUFF INFANT RESUSCITATOR
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTL·February 1, 2012
DEPUY HIP REPLACEMENT
FDA Adverse Event
Injury
·DEPUY·Product code LPH·May 19, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013