2,940 results · 23ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

CLARITY

FDA 510(k)
FDA Class 2 ·Radiology

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B16741418550·

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B1674141855060·

EBERLE

FDA UDI
Eberle GmbH & Co. KG·04050052016043·Tapered Burr 5,5

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X1418550·14mm H x 18mm W x 55mm L x 0 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X14185580·14mm H x 18mm W x 55mm L x 8 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587L141855120·14mm H x 18mm W x 55mm L XLIF Trial 12 degree L...

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X141855120·14mm H x 18mm W x 55mm L x 12 degrees XLIF

Zavation

FDA UDI
Zavation LLC·00842166150591·14x18x55mm, 6°, MILC

Zavation

FDA UDI
Zavation LLC·00842166154179·14x18X55mm, 12°, MILC

ZEUS-L

FDA UDI
SPINAL ELEMENTS·00840916121662·ZEUS®-L Implant, 14 x 18 x 55mm, Parallel

Zavation

FDA UDI
Zavation LLC·00842166149847·14x18x55mm, 0°, MILC

ZEUS-L

FDA UDI
SPINAL ELEMENTS·00840916121648·ZEUS®-L Implant, 14 x 18 x 55mm, Lordotic

PLEATS PLUS N95 PARTICULATE RESPIRATOR, MODELS 1050 AND 1050S

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

PROFAST+ ASSAY

FDA 510(k)
FDA Class 2 ·Microbiology

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 27, 2011

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 27, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 20, 2021