2,954 results · 23ms · Sources: EU EUDAMED, US FDA

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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