2,954 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
RESPROCESSED SERFAS ENERGY PROBE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741218550·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674121855060·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1218550·12mm H x 18mm W x 55mm L x 0 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X121855120·12mm H x 18mm W x 55mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L121855120·12mm H x 18mm W x 55mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X12185580·12mm H x 18mm W x 55mm L x 8 degrees XLIF
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916121372·ZEUS®-L - 12x18x55mm
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916121396·ZEUS®-L Implant, 12 x 18 x 55mm, Parallel
Zavation
FDA UDI
Zavation LLC·00842166149830·12x18x55mm, 0°, MILC
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916121389·ZEUS®-L Implant, 12 x 18 x 55mm, Lordotic
Arthrex®
FDA UDI
ARTHREX, INC.·00888867087804·DRILL, 5.5MM CANNULATED
Zavation
FDA UDI
Zavation LLC·00842166154162·12x18X55mm, 12°, MILC
Zavation
FDA UDI
Zavation LLC·00842166150584·12x18x55mm, 6°, MILC
TOP GLOVE POWDERFREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELLING CLAIMS (50 MICROGRAMS OR LESS)
FDA 510(k)
FDA Class 1
·General Hospital
PROFAST+ ASSAY
FDA 510(k)
FDA Class 2
·Microbiology
WAVELIGHT EX500 EXCIMER LASER
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·May 15, 2013
STANDARD STRETCHER
FDA Adverse Event
Malfunction
·HILLROM DE MEXICO S DE RL DE CV·Product code FPO·July 31, 2014
LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (SMALL)
FDA Adverse Event
Malfunction
·ALLERGAN·Product code LTI·May 20, 2011
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 27, 2021