30 results · 22ms · 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.

WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Bur PM2-95 80K Diam Ø5.0 St

FDA UDI
Bien-Air Surgery SA·17630055514889·

CoRoent

FDA UDI
Nuvasive, Inc.·00887517285454·CoRoent XL-H Trial, 8mm 20°

Endo Carry-On Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964055393·Endo Carry-on Procedure Kit includes Suction Tu...

TI LOW PROFILE SCREW 6.5X25MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 28, 2017

E-POLY 36MM +3 HIWALL LNR SZ23

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·September 28, 2017

TI LOW PROFILE SCREW 6.5X20MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 28, 2017

TI LOW PROFILE SCREW 6.5X25MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 28, 2017

R/B RLOC LHOLE SHL 50MM SZ 23

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·September 28, 2017

V.A.T.S. HARKEN DEBAKEY CLAMP

FDA UDI
SONTEC INSTRUMENTS, INC.·B09921008200·V.A.T.S. HARKEN DEBAKEY CLAMP WITHOUT RATCHET M...

V.A.T.S. HARKEN DEBAKEY CLAMP

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896003569·V.A.T.S. HARKEN DEBAKEY CLAMP WITHOUT RATCHET M...

DX SERIES FINGER SENSOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

AVANAR F/X 2.9F INTRAVASCULAR ULTRASOUND IMAGING CATHETER, MODEL 85700

FDA 510(k)
FDA Class 2 ·Cardiovascular

N/A

FDA UDI
Doppkon GmbH & Co. KG·04262494463693·Curette forward angled D 3mm, L 5mm, WL 120mm

LEONE SPA

FDA UDI
LEONE SPA·08033707102502·SLEEVES FOR GUIDED SURGERY FOR TAD

Scan Post

FDA UDI
BICON, LLC·00813110029751·2.5mm Titanium Scan Post (2)

Widex

FDA UDI
Widex A/S·05706069727678·Widex EVOKE E-FA (Summer gold S-440 ) Telecoil,...

Widex

FDA UDI
Widex A/S·05706069727272·Widex EVOKE E-FM (Summer gold S-440 ) RC coil

Widex

FDA UDI
Widex A/S·05706069729672·Widex EVOKE E-FP (Summer gold S-440 ) Telecoil,...

PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code LWP·June 10, 2015