7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANSPACH SHIELDED ATTACHMENT
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
2ND MODIFIED VINYLAC PRESS PACK DENTURE RESIN
FDA 510(k)
FDA Class 2
·Dental
MYOTRACK, MODEL HH 515
FDA 510(k)
FDA Class 2
·Anesthesiology
LAG SCREW STEP DRILL GAMMA3 Ø10.5X495 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·February 22, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 1, 2014
Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026