37 results · 24ms · 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.

FitboneTM Trochanteric

FDA 510(k)
FDA Class 2 ·Orthopedic

Flair Toothbrush

FDA UDI
SAFCO DENTAL SUPPLY CO.·10810063755949·Flair Toothbrush, contoured power point tip, cr...

APEX Revision Knee

FDA UDI
Omni Life Science, Inc.·00841690124764·Modular Stem 11mm x 125mm

Bradshaw Medical Inc.

FDA UDI
Bradshaw Medical, Inc.·00810019930904·BIT, HEX MALE 9/64 1/4 SQ

Kleiner KG2 system

FDA UDI
Baat Medical Products B.V.·08720246782790·Trial

PRO FIT DISPOSABLE RECTAL SPECULUM, MODELS 8116 AND 8117

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

HS AMICA DEVICES FAMILY

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

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 25, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 3, 2024

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 19, 2025

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 21, 2024

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 12, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 17, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 26, 2024

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 20, 2025

INTERMATE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·November 14, 2014

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·September 15, 2011

OXIMAX ADULT OXYGEN SENSOR

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY TYCO·Product code NLF·July 23, 2013