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RESPONSIVE ARTHROSCOPY

FDA registration
RESPONSIVE ARTHROSCOPY·6 products·🇺🇸 United States

Responsive Arthroscopy

FDA UDI
Provision·B504OM9050010020·

Responsive Arthroscopy

FDA UDI
Provision·B504OM90700108500·

Responsive Arthroscopy Thunderbolt System

FDA 510(k)
FDA Class 2 ·Orthopedic

Responsive Arthroscopy Interference Screw System

FDA 510(k)
FDA Class 2 ·Orthopedic

Responsive Arthroscopy Suture Anchor System

FDA 510(k)
FDA Class 2 ·Orthopedic

Responsive Arthroscopy Suture Anchor System

FDA 510(k)
FDA Class 2 ·Orthopedic

Responsive Arthroscopy Interference Screw System

FDA 510(k)
FDA Class 2 ·Orthopedic

Responsive Arthroscopy Wedge Push-In Suture Anchors

FDA 510(k)
FDA Class 2 ·Orthopedic

Responsive Arthroscopy Wedge Push-In Suture Anchors

FDA 510(k)
FDA Class 2 ·Orthopedic

Responsive Arthroscopy Mustang and Mustang Knotless Suture Anchors

FDA 510(k)
FDA Class 2 ·Orthopedic

Responsive Arthroscopy Stealth and Mini Stealth All-Suture Anchors

FDA 510(k)
FDA Class 2 ·Orthopedic

101 DRAINAGE CANNULA WITH TROCAR

FDA Adverse Event
Injury ·RICHARD WOLF MEDICAL INSTRUMENTS·Product code HIF·December 17, 2012

FMS DUO +

FDA Adverse Event
DEPUY MITEK·Product code HRX·September 1, 2010

R. WOLFE 101 DRAINAGE CANNULA WITH TROCAR

FDA Adverse Event
RICHARD WOLF MEDICAL INSTRUMENTS·Product code HRX·December 19, 2012

CARDINAL HEALTH

FDA Adverse Event
Malfunction ·CARDINAL HEALTH 200, LLC·Product code OJH·November 26, 2024

*

FDA Adverse Event
*·Product code HRX·September 2, 2011

FORMULA TOMCAT

FDA Adverse Event
STRYKER ENDOSCOPY·Product code HRX·June 17, 2010

DYONICS INCISOR PLUS ELITE

FDA Adverse Event
Malfunction ·SMITH & NEPHEW·Product code HRX·September 23, 2012

MEMORY

FDA Adverse Event
Malfunction ·HOWMEDICA OSTEONICS CORP., AKA STRYKER ORTHOPAEDICS·Product code JDR·January 12, 2016