26 results · 24ms · Sources: EU EUDAMED, US FDA

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NobelProcera Zirconia Implant Bridge

FDA 510(k)
FDA Class 2 ·Dental

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113424·CRESCENT KNIFE BEVEL UP (BX/5)

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112878·CORNEAL TREPHINE BLADE6.5MM

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112465·BARRON VACUUM TREPHINE 6.5MM

PORTA OP SOLDER M-1

FDA 510(k)
FDA Class 2 ·Dental

3M RELY X VENEER CEMENT TRY-IN PASTER

FDA 510(k)
FDA Class 2 ·Dental

BIOPSY AND GRASPING FORCEPS, 5 FR.

FDA Adverse Event
Malfunction ·KARL STORZ SE & CO. KG·Product code GCJ·May 1, 2025

VITROS ECI IMMUNODIAGNOSTIC SYSTEM

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·October 8, 2008

UNKNOWN TRIDENT ACETABULAR SYSTEM

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS CORK·Product code LPH·August 5, 2011

IMMULITE 2000 PROSTATE SPECIFIC ANTIGEN

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code MTF·July 2, 2013

COBAS E 402 ANALYTICAL UNIT

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·December 17, 2024

MEDTRONIC LEAD

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·July 9, 2024

ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

FDA Adverse Event
Death ·BOSTON SCIENTIFIC CORPORATION·Product code MCX·April 30, 2026

ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MCX·April 30, 2026

SENSOR UROLOGICAL GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EZB·May 29, 2025

MEDTRONIC IPG

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·July 9, 2024

MEDTRONIC LEAD

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·July 9, 2024

BENCHMARK SPECIAL STAINS SYSTEM

FDA Adverse Event
Injury ·VENTANA MEDICAL SYSTEMS INC.·Product code KPA·August 21, 2025

MERSILENE TAPE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAT·November 12, 2024

ALINITY I STAT HIGH SENSITIVE TROPONIN-I REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code MMI·February 18, 2026