8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LAZER-TRACH TRACHEAL TUBE
FDA 510(k)
FDA Class 2
·Anesthesiology
PERITONEAL DIALYSIS
FDA Adverse Event
Injury
·UNKNOWN·Product code FKX·August 12, 2023
GEISTLICH BIO-OSS, GEISTLICH BIO-OSS COLLAGEN, GEISTLICH COMBI-KIT COLLAGEN, GEISTLICH PERIO SYSTEM COMBI PACK, GEISTLIC
FDA 510(k)
FDA Class 2
·Dental
EPICOR MEDICAL ABLATION SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CMW 3 BONE CEMENT 40 G
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS·Product code LOD·January 8, 2020
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 18, 2013
CAPSURE SP NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010
ACCU-CHEK ® MOBILE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 9, 2014