174 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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