32 results · 38ms · 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.

Hintermann Series H2 Total Ankle System

FDA 510(k)
FDA Class 2 ·Orthopedic

NA

FDA UDI
KEY SURGICAL, INC.·00849771048183·K-Wire and Steinmann Pin Dispensers, .054-inch...

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704292251·DISP K-WIRE FOR .054" (1.4MM) 6.25"

Facebow

FDA UDI
ORMCO CORPORATION·00889989079784·Facebow ,REG OB,STD MED IB, 045

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001171·Invue Max, Two Level ACP, 49mm

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001201·Invue Max, Two Level ACP, 55mm

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001195·Invue Max, Two Level ACP, 53mm

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001157·Invue Max, Two Level ACP, 45mm

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001119·Invue Max, Two Level ACP, 37mm

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001126·Invue Max, Two Level ACP, 39mm

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001096·Invue Max, Two Level ACP, 33mm

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001188·Invue Max, Two Level ACP, 51mm

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001140·Invue Max, Two Level ACP, 43mm

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001102·Invue Max, Two Level ACP, 35mm

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001164·Invue Max, Two Level ACP, 47mm

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001133·Invue Max, Two Level ACP, 41mm

OSTEOCRETE BONE VOID FILLER

FDA 510(k)
FDA Class 2 ·Orthopedic

ATLANTIS ABUTMENT FOR DENTSPLY ANKYLOS IMPLANT, ATLANTIS GEMINI ABUTMENT, ATLANTIS GEMINI + ABUTMENT

FDA 510(k)
FDA Class 2 ·Dental

PERSONA®

FDA UDI
Zimmer, Inc.·00889024238619·

FT4, FREE THYROXINE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·November 13, 2017