12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNERMED ALT/GPT REAGENT KIT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
RIWO-ART
FDA UDI
Richard Wolf GmbH·04055207022122·TROCAR SLEEVE STRAI. CAP 5.5MM WL 150MM stainl...
WRIST FIT
FDA UDI
Stryker GmbH·00886385000091·Ulnar Column Plate
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690115410·Retaining Bolt PS or PS-C Insert, Modular Tibia...
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471150584·K-WIRE - DOUBLE TROCAR 1.0mm DIA x 150mm
RANGE SPINAL SYSTEM (MESA AND DENALI)
FDA 510(k)
FDA Class 2
·Orthopedic
AMX-4 PLUS MOBILE X-RAY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·January 17, 2013
HANDLES & CONNECTOR WITH DISCHARGE CONTROL FOR INTERNA
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code LDD·December 7, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 9, 2014
Allura Xper FD10 Product Codes: (1)722010, (2) 722026, (3) 722003; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·October 1, 2025
Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025