33 results · 23ms · Sources: EU EUDAMED, US FDA

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HEMO-Bandage

FDA 510(k)
FDA Unclassified ·Unknown

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772813841·GENUMEDI PRO SILVER SIZE IV

LinkSymphoKnee

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575289820·Tibial Cutting Block, right

BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM CEFEPIME (STREP) 0.0625-4UG/ML

FDA 510(k)
FDA Class 2 ·Microbiology

MEG-2 BLOOD GLUCOSE MONITORING SYSTEM, MEG-2 50'S TEST STRIP, MEG-2 CONTROL SOLUTION

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

VACUTRON

FDA UDI
Allied Medical, LLC·00026072007754·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

BD PHOENIX¿ SMIC-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026

VACUTRON

FDA UDI
Allied Medical, LLC·00026072007808·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072007778·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072007785·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072007761·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072007792·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·June 26, 2024

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

UNKNOWN DEPUY 36 + 1.5 HEAD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·June 30, 2011

DAMON COPPER NITI WIRE

FDA Adverse Event
Malfunction ·ORMCO CORPORATION·Product code DZC·September 9, 2008

BD PHOENIX¿ SMIC/ID-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024

BD PHOENIX¿ SMIC/ID-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 1, 2024

ADVANCE 35 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code DQY·February 3, 2017

BD PHOENIX¿ SMIC-101

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025