84 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.

CamX Triton HD Proxi Head

FDA 510(k)
FDA Class 2 ·Dental

External Fixation

FDA UDI
Life Spine, Inc.·00190837023720·Oblique Support

Ophthalmic Ring

FDA UDI
KATENA PRODUCTS, INC.·00841668100813·FLIERINGA FIXATION RING 20MM

Arena-C

FDA UDI
SPINEFRONTIER, INC.·00190361023142·Arena-C HA, 12x15, Straight 12mm

Arena-C

FDA UDI
SPINEFRONTIER, INC.·00190361023135·Arena-C HA, 12x15, Straight 11mm

Arena-C

FDA UDI
SPINEFRONTIER, INC.·00190361023067·12x15 Arena-C PEEK HA Straight 5mm

Arena-C

FDA UDI
SPINEFRONTIER, INC.·00190361023050·12x15 Arena-C PEEK HA Straight 6mm

Arena-C

FDA UDI
SPINEFRONTIER, INC.·00190361023036·12x15 Arena-C PEEK HA Straight 8mm

Arena-C

FDA UDI
SPINEFRONTIER, INC.·00190361023043·12x15 Arena-C PEEK HA Straight 7mm

Arena-C

FDA UDI
SPINEFRONTIER, INC.·00190361023128·Arena-C HA, 12x15, Straight 10mm

Arena-C

FDA UDI
SPINEFRONTIER, INC.·00190361023029·12x15 Arena-C PEEK HA Straight 9mm

CARTO 3 EP NAVIGATION SYSTEM, VERSION 2.2

FDA 510(k)
FDA Class 2 ·Cardiovascular

PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,

FDA 510(k)
FDA Class 2 ·Anesthesiology

Persona® The Personalized Knee®

FDA UDI
Zimmer, Inc.·00889024238756·

RIVA STAR SILVER DIAMINE FLUORIDE

FDA Adverse Event
Injury ·SDI LIMITED·Product code LBH·February 13, 2019

SANTORINI™ Corpectomy Cage System

FDA UDI
VB Spine LLC·10888857243071·Footprint Trial, Size 12x14 mm

SANTORINI™ Corpectomy Cage System

FDA UDI
VB Spine LLC·10888857243088·Footprint Trial, Size 12x17 mm

PUSHING CATHETER

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·October 19, 2022

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011