27 results · 21ms · Sources: EU EUDAMED, US FDA

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g.Nautilus PRO

FDA 510(k)
FDA Class 2 ·Neurology

Key Surgical K-Wires and Steinmann Pins

FDA UDI
KEY SURGICAL, INC.·00849771015109·Steinmann Pins, Single diamond, round end, 1/8-...

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704293814·

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·14026704912466·

NA

FDA UDI
KEY SURGICAL, INC.·10849771049958·Steinmann Pins, Single diamond, round end, 1/8-...

mahe medical GmbH

FDA UDI
mahe medical gmbh·04050659485198·Steinmann pin w. lanzet/round end _x000D_...

Steinmann pin w. lanzet/round end 3.2mm/229mm, 6 pcs./unit

FDA UDI
mahe medical gmbh·EMAHKM716690·Steinmann pin w. lanzet/round end 3.2mm/...

M.U.S.T. MINI POLYAXIAL SCREW

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·August 27, 2025

MUST MINI POLYAXIAL SCREW 3.5 X 12 FULL THREAD + NUT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·April 6, 2018

MUST MINI POLYAXIAL SCREW 3.5 X 12 FULL THREAD + NUT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·March 8, 2022

THERMODILUTION CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

INTEGRA SELECTOR ULTRASONIC SURGICAL ASPIRATOR SYSTEM WITH BONE TIP

FDA 510(k)
FDA Unclassified ·Unknown

MUST MINI ROD TI 3.5 X 80MM (STERILE)

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·July 13, 2021

BD NANO PRO ULTRA-FINE¿ PEN NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·April 4, 2019

MUST MINI MUST MINI POLYAXIAL SCREW 3.5 X 24 FULL THREAD + NUT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·July 14, 2020

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 21, 2011

SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 15, 2013

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·October 14, 2014

PERFORMER INTRODUCER

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·April 15, 2022

PERFORMER INTRODUCER

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·September 11, 2024