31 results · 22ms · Sources: EU EUDAMED, 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