41 results · 22ms · Sources: EU EUDAMED, US FDA

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Self-retaining Retractor

FDA 510(k)
FDA Class 2 ·Neurology

Cohere

FDA UDI
Nuvasive, Inc.·00195377028136·COHERE TLIF-O Trial, 16x10mm 4°

OsteoMed

FDA UDI
OSTEOMED LLC·00845694033985·Logic Jr. 52mm Right Short Distractor,15mm Dist...

Sentry Dental TC&B

FDA UDI
NU RADIANCE INC·00815143001933·Sentry Dental TC&B Shade A3

Vilex Power Accessory

FDA UDI
VILEX IN TENNESSEE, INC.·00841731122254·KWire .062x4" (1.6x100mm)

UniTip Catheter

FDA UDI
Unisensor AG·07640172973226·

HANSEN MEDICAL VASCULAR CATHETER CONTROL SYSTEM AND CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

ATLANTIS ABUTMENT FOR DENTSPLY ANKYLOS IMPLANT, ATLANTIS GEMINI ABUTMENT, ATLANTIS GEMINI + ABUTMENT

FDA 510(k)
FDA Class 2 ·Dental

CARELINK

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code KRG·October 10, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 17, 2011

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·September 11, 2022

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·April 14, 2026

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·May 24, 2021

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·January 11, 2022

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·January 29, 2026

SHIRANUI HP

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·May 18, 2020

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·October 22, 2024

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

SHIRANUI HP

FDA Adverse Event
Malfunction ·KANEKA CORPORATION·Product code LIT·April 24, 2019