80 results · 30ms · Sources: EU EUDAMED, US FDA

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REPEL SURGICAL GLOVE LINERS

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

Instruments

FDA UDI
Nuvasive, Inc.·00887517385147·ALGI Curette, Straight Medium

Tibial Spacer

FDA UDI
ADLER ORTHO SPA·08052693620555·10 mm LB TIBIAL SPACER

Peerless Buccal Tube

FDA UDI
ORMCO CORPORATION·00889989022650·ASSY ORTHOS A/P SGL -4LFM -10X18 LR

Mariner

FDA UDI
Seaspine Orthopedics Corporation·10889981129484·Set Screw Starter, 1/4 sq

TOTALSHIELD®

FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024376441·Zippered Surgical Toga, Regular

Intervertebral Body Fusion Device

FDA UDI
PRECISION SPINE, INC.·00840019923309·TLIF Sizer 10mm x 24mm

VOYAGER 6.0 SOFTWARE OPTION

FDA 510(k)
FDA Class 2 ·Neurology

EQUIVABONE

FDA 510(k)
FDA Class 2 ·Orthopedic

FLEXCATH CONTOUR¿ STEERABLE SHEATH

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code DRA·June 11, 2025

FLEXCATH CONTOUR¿ STEERABLE SHEATH

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code DRA·October 3, 2025

FLEXCATH CONTOUR¿ STEERABLE SHEATH

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code DRA·August 27, 2025

FLEXCATH CROSS TRANSSEPTAL SOLUTION

FDA Adverse Event
Injury ·ACUTUS MEDICAL INC·Product code DYB·November 4, 2025

FLEXCATH CONTOUR¿ STEERABLE SHEATH

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code DRA·December 10, 2024

FLEXCATH CONTOUR¿ STEERABLE SHEATH

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code DRA·December 10, 2024

INTERSTIM II

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 27, 2014

SCREW

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·January 7, 2013

CELL-DYN EMERALD DILUENT

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·November 16, 2010

PULSESELECT

FDA Adverse Event
Injury ·MEDTRONIC CRYOCATH LP·Product code QZI·March 23, 2026

FLEXCATH CONTOUR¿ STEERABLE SHEATH

FDA Adverse Event
Injury ·MEDTRONIC CRYOCATH LP·Product code DRA·March 23, 2026