46 results · 27ms · Sources: EU EUDAMED, US FDA

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GYNEFLEX

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

BUSCH®, BNA®

FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120211151·Carbide, cylinder round, amalgam remover, blue ...

PEDICLE SCREW 7X45

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·April 10, 2018

Reicodent

FDA UDI
devemed GmbH·04061644051410·Mouth Gag "Molt mod." | 11 cm with tongue depre...

Reicodent

FDA UDI
devemed GmbH·04061644046119·Mouth Gag "Molt" | 14 cm

Reicodent

FDA UDI
devemed GmbH·04061644046102·Mouth Gag "Molt" | 11 cm

Reicodent

FDA UDI
devemed GmbH·04061644051427·Mouth Gag "Molt mod." | 14 cm with tongue depre...

PEDICLE SCREW 7X50

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 23, 2018

PEDICLE SCREW 5X45

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·March 23, 2018

BLUEENDO

FDA UDI
TROKAMED GmbH·04251303812074·Cutting module Ø 12,5mm for Morcellator System...

ULTRA CATHETER SET

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

KURZ UPPER EYELID IMPLANT- PLATINUM/IRIDIUM,MODELS REGULAR 4007 003-007, SPECIAL 4007 002, 4007 008-010

FDA 510(k)
FDA Class 2 ·Ophthalmic

M.U.S.T. RODS

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·April 20, 2026

PEDICLE SCREW PEDICLE SCREW 5X40

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·January 17, 2024

M.U.S.T. POLYAXIAL PEDICLE SCREW

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·October 28, 2024

MUST PEDICLE SCREW 8X40MM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 22, 2017

PEDICLE SCREW - PEDICLE SCREW 8X75MM

FDA Adverse Event
Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·October 11, 2018

PEDICLE SCREW PEDICLE SCREW 7X45

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·September 9, 2022

UNKNOWN TICRON

FDA Adverse Event
Injury ·DAVIS & GECK CARIBE LTD·Product code GAT·October 13, 2021

MECTALIF OBLIQUE (TI PEEK) INTERBODY FUSION DEVICE 12X28X11 L10

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·April 1, 2020