16 results · 29ms · 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.

AEON Endoscopic Stapler

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

HEALIX PEEK ORTHOCORD

FDA UDI
Medos International Sàrl·10886705007585·HEALIX PEEK Anchor w/ORTHOCORD and Needles PEEK...

LEONE SPA

FDA UDI
LEONE SPA·08033707066439·LIGAT SLIDE LOW FRICTION ICE MEDIUM

APEX PS Knee

FDA UDI
Omni Life Science, Inc.·00841690113492·PS-C Insert, Size 2 x 10mm

restor3d Utility Wedge

FDA UDI
Restor3d, Inc.·00840097505039·Ti Anatomic Evans Wedge, Large Footprint, 10mm ...

Steerable IBD

FDA UDI
Seaspine Orthopedics Corporation·10889981117320·Fixed Rasp; 22x10 (05-3300)

Empower Clear

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746154447·COSMETIC SL EMPOWER CLEAR INTERACT UL LAT 022 T...

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B167310222210110·

ZAVATION ROD CONNECTOR

FDA UDI
Zavation LLC·00197157016623·ROD CONNECTOR, PARALLEL SIDE LOADING 10mm offse...

Empower Clear

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746000782·COSMETIC SL EMPOWER CLEAR INTERACT UL LATERAL 0...

Empower Clear Bracket

FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746200328·COSMETIC SL EMPOWER CLEAR INTERACT UL LAT 022 T...

MULTIFUNCTIONAL ELECTRODE MODELS 9640, 9650

FDA 510(k)
FDA Class 3 ·Cardiovascular

NEWFIX EXTERNAL FIXATION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ARTHREX

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code HXI·November 5, 2008

ULTRATOME¿

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FDI·August 24, 2011

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 12, 2013