21 results · 24ms · Sources: EU EUDAMED, US FDA

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UCP Drug Test Mini Cups

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

n.a.

FDA UDI
Karl Storz GmbH & Co. KG·04048551057575·Cotton Applicator, with thread, 17.5 cm

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575291182·Knee femur prosthesis trial - Endo Model Knee S...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575290970·Knee femur prosthesis trial - Endo Model Knee S...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575290833·Knee femur prosthesis trial - Endo Model Knee S...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575290659·Knee femur prosthesis trial - Endo Model Knee S...

GRANDIO FLOW

FDA 510(k)
FDA Class 2 ·Dental

PRECISION XTRA PLUS OR OPTIUM PLUS, BLOOD GLUCOSE TEST STRIPS

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008195·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008188·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008201·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008218·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

VACUTRON

FDA UDI
Allied Medical, LLC·00026072008171·CONTINUOUS / INTERMITTENT SUCTION REGULATORS

ILAB? POLARIS MULTI-MODALITY GUIDANCE SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·May 14, 2026

OT PING METER

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

DAMON COPPER NITI WIRE

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

ALTRX +4 10D 32IDX48OD

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

D902 LILLIPUT ECMO M PHISIO

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·April 7, 2022

LILLIPUP PMP, LILLIPUT PMP INTEGRATED

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·June 27, 2022

ULTRACISION HARMONIC ACE (EXACT CODE UNKNOWN)

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 26, 2019