25 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Tornier Perform Humeral System Stemless
FDA 510(k)
FDA Class 2
·Orthopedic
ambIT* Introducer - Beveled Tip, Peelable Sheath
FDA UDI
Avanos Medical, Inc.·00193494000615·ambIT* Introducer - Beveled Tip, Peelable Sheath
ambIT
FDA UDI
SUMMIT MEDICAL PRODUCTS, INC.·00857595005022·Introducer- 8 inch
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113263·PS Insert, Size 4 x 18mm
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·34546540355653·Bone Screws, Cross-Pin
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220418070·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220418000·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220418150·
ELECTROSUGRICAL RESECTION AND VAPORIZATION ELECTRODE SERIES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES
FDA 510(k)
FDA Class 2
·General Hospital
VERSACROSS CONNECT LAAC ACCESS SOLUTION
FDA Adverse Event
Injury
·BAYLIS MEDICAL COMPANY INC.·Product code DRE·April 6, 2023
HF-RESECTION ELECTRODE, FOR TURIS
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code FAS·February 9, 2023
HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, MEDIUM, 12°
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code FAS·September 4, 2024
CAPIO OPEN ACCESS SUTURE CAPTURING DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FHQ·October 31, 2008
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·August 23, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013
HF-RESECTION ELECTRODE, LOOP
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code FAS·March 28, 2023
HF-RESECTION ELECTRODE
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code FAS·December 28, 2022
HF-RESECTION ELECTRODE, LOOP
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code FAS·April 27, 2023
BD RAPID DETECTION OF SARS-COV-2 VERITOR
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·November 6, 2020