31 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INION CPS BABY 1.5 BIOABSORBABLE FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Dental
ACE Surgical
FDA UDI
Prismatik Dentalcraft, Inc·D74530103510·ACE Surgical TRI-CAM Scanning Abutment Anterior...
ACE Surgical
FDA UDI
Prismatik Dentalcraft, Inc·D74520103510·ACE Surgical INTERNAL HEX Scanning Abutment, 3....
INTERNAL HEX
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950027231·INTERNAL HEX SCANNING ABUTMUNT 3.5MM PLATFORM 1...
TRI-CAM Dental Implant System
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950027507·TRI-CAM SCANNING ABUTMENT 3.5MM ANTERIOR
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756000833·Cervical Collar
RESPONDER 5, INTERACTIVE
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828195195·
AutoPose Restore
FDA UDI
PUREGRAFT LLC·00850009190130·A sterile, single use microsizing syringe syste...
AutoPose Restore
FDA UDI
Bimini Technologies LLC·00850034511276·A sterile, single use microsizing syringe syste...
INSET II
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 30, 2026
INSET II
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 30, 2026
INSET II
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 30, 2026
INSET II
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 30, 2026
POLY-TAPES WITH THE FASTLOK FIXATION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE
FDA 510(k)
FDA Class 1
·General Hospital
INSET II
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·October 9, 2025
INSET II
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·October 9, 2025
AXSYM DIGOXIN III
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007
ES2 INTEGRATED BLADE SCREW SIZE L 6.5X50MM
FDA Adverse Event
Malfunction
·STRYKER SPINE-FRANCE·Product code NKB·March 19, 2013
ACCU-CHEK ® COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 8, 2011