1,600 results · 27ms · 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.

TITE-FIT/TAPERED TITE-FIT

FDA UDI
HI-TEC IMPLANTS LTD.·07290110727468·IMPLANT ANALOG

APK

FDA UDI
APK Technology Co.,Ltd.·06946725502952·LDW DIN 3-LD Set, SNAP to DIN, AHA,24"

APK

FDA UDI
APK Technology Co.,Ltd.·06946725503003·LDW DIN 5-LD Set, SNAP to DIN,AHA,24"

APK

FDA UDI
APK Technology Co.,Ltd.·06946725503010·LDW DIN 5-LD Set, SNAP to DIN, AHA, 40"

APK

FDA UDI
APK Technology Co.,Ltd.·06946725503027·LDW DIN 5-LD Set, PINCH to DIN, AHA, 18"

APK

FDA UDI
APK Technology Co.,Ltd.·06946725502976·LDW DIN 3-LD SET, PINCH TO DIN, AHA, 24"

APK

FDA UDI
APK Technology Co.,Ltd.·06946725503034·LDW DIN 5-LD Set, PINCH to DIN, AHA, 24"

APK

FDA UDI
APK Technology Co.,Ltd.·06946725502945·LDW DIN 3-LD Set, SNAP to DIN,AHA,18"

APK

FDA UDI
APK Technology Co.,Ltd.·06946725503041·LDW DIN 5-LD Set, PINCH to DIN, AHA, 40"

APK

FDA UDI
APK Technology Co.,Ltd.·06946725502969·LDW DIN 3-LD Set, SNAP to DIN, AHA,40"

APK

FDA UDI
APK Technology Co.,Ltd.·06946725502990·LDW DIN 5-LD Set, SNAP to DIN,AHA,18"

APK

FDA UDI
APK Technology Co.,Ltd.·06946725502983·LDW DIN 3-LEAD SET- PINCH TO DIN,AHA

VERIFYNOW

FDA Adverse Event
Injury ·WERFEN COMPANY/ACCRIVA DIAGNOSTIC, INC.·Product code JOZ·December 28, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 22, 2020

Adaptor, Grooming

FDA classification
FDA Class 1 ·Adaptor, Grooming

Raphael 707-PR

Device
EU MDR · Eu Md Class 1 ·YOUNG IL M Co., Ltd.·On the market·1 country

HLW Dentalinstruments GmbH

Manufacturer
🇩🇪 Germany

YOUNG IL M Co., Ltd.

Manufacturer
🇰🇷 South Korea·1 Basic UDI-DI·1 Device

GLW, Inc.

FDA registration
GLW, Inc.·22 products·🇺🇸 United States

ILC Dover

FDA registration
ILC Dover·1 product·🇺🇸 United States