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

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ELECSYS PROBNP IMMUNOASSAY

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526827943·ACHIMED ACHILLES SUPP BLACK VI

APEX PS Knee

FDA UDI
Omni Life Science, Inc.·00841690113744·PS-C Insert, Size 5 x 16mm

6mm Aspiration Kit

FDA UDI
MEDGYN PRODUCTS, INC.·M803022516·6mm Aspiration Kit

CARE IFC PLUS

FDA 510(k)
FDA Class 2 ·Neurology

EBI SPINELINK - II SPINAL FIXATION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

DEXCOM FOLLOW APP

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·January 27, 2025

audifon

FDA UDI
audifon GmbH & Co. KG·EADF0225168701315917201·BTE

audifon

FDA UDI
audifon GmbH & Co. KG·EADF0225168701312717201·BTE

audifon

FDA UDI
audifon GmbH & Co. KG·EADF0225168701312017201·BTE

audifon

FDA UDI
audifon GmbH & Co. KG·EADF0225168701338117201·BTE

audifon

FDA UDI
audifon GmbH & Co. KG·EADF022516870133217201·BTE

audifon

FDA UDI
audifon GmbH & Co. KG·EADF022516870131217201·BTE

audifon

FDA UDI
audifon GmbH & Co. KG·EADF022516870132517201·BTE

audifon

FDA UDI
audifon GmbH & Co. KG·EADF022516870131317201·BTE

audifon

FDA UDI
audifon GmbH & Co. KG·EADF0225168701338217201·BTE

DRILL, 2.75MM, .066 CANNULATION

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MDM·October 27, 2025

COTTON-LEUNG BILIARY STENT

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·March 20, 2013

INRATIO

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·February 15, 2011

ACCU-CHEK COMPLETE

FDA Adverse Event
Injury ·ROCHE DIAGNOSTICS·Product code NBW·April 1, 2008