174 results · 22ms · Sources: EU EUDAMED, US FDA

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PARTIAL OSSICULAR REPLACEMENT PROSTHESES

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

TruForm

FDA UDI
Rmo, Inc.·00885797099938·R&L MAX MOLAR 214 BDS W/O LUGS

Mini-Mono®

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70605181·Mini-Mono-Brackets Roth 'N' .018" 200 Brackets ...

Symmetry Surgical

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482048788·Symmetry® Forceps, Tissue, 1x2 Teeth, 7 in

SYNTHES ANTEROLATERAL CALCANEAL PLATE

FDA 510(k)
FDA Class 2 ·Orthopedic

MACROPRO GEL

FDA 510(k)
FDA Unclassified ·Unknown

BD PHOENIX PMIC110

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·October 19, 2021

BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·August 23, 2021

BD PHOENIX PANEL PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 10, 2023

BD PHOENIX PANEL PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 10, 2023

BD PHOENIX¿ PMIC/ID-106

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025

BD PHOENIX¿ PMIC/ID-106

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025

BD PHOENIX¿ PMIC/ID-106

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·April 15, 2024

BD PHOENIX¿ PMIC/ID-106

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 23, 2024

BD PHOENIX¿ PMIC/ID-106

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 26, 2024

BD PHOENIX¿ PMIC/ID-106

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 26, 2024

11.0 CM LONG ATTACHMENT

FDA Adverse Event
Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·April 10, 2013

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·April 18, 2011

S4 SET SCREW NEW VERSION

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code KWP·June 11, 2008

BD PHOENIX¿ PMIC/ID-106

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 27, 2024