31 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ANESTHESIA CONDUCTION NEEDLES
FDA 510(k)
FDA Class 2
·Anesthesiology
One
FDA UDI
GLOBAL PROTECTION CORP.·00726893115125·ONE Flex 3-Pack,
Pro-Link Ti
FDA UDI
Life Spine, Inc.·00190837080877·
Pro-Fit
FDA UDI
PULMODYNE INC·00841470111267·
MIRABAY
FDA UDI
Mirabay Orthodontics Corp.·05061075029261·OPTIMAL SYMMETRY ARCHWIRE TRANS THERM PL W/STOP...
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00840180517925·ALIF, MODULAR DISTRACTOR, IMPACTION TIP, 6mm, S...
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001011310060·OneLIF Interbody, Small, 13 Degree, 10mm X 6mm
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311310060·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321310060·
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001111310060·Trial-OneLIF Interbody, Small, 13 Degree, 10mm ...
CI-SNAP WOUND CARE SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
WAVELIGHT FS200 LASER SYSTEM MODEL: FS200
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OneLIF™
FDA UDI
Novapproach Spine LLC·G070010113100620·OneLIF Cage, Small, 13 Degree, 10mm X 6mm - Obl...
COOK® CERVICAL RIPENING BALLOON
FDA Adverse Event
Malfunction
·COOK INC·Product code PFJ·July 18, 2016
OneLIF™
FDA UDI
Novapproach Spine LLC·G070SPX01161310060·Special Instrument Starter Trial, Medium, 13deg...
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
COOK® CERVICAL RIPENING BALLOON
FDA Adverse Event
Malfunction
·COOK INC·Product code PFJ·July 19, 2016
TOTAL ASR ACET IMP SIZE 54
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD.-8010379·Product code KWA·October 1, 2014