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Pure-Vu

FDA UDI
MOTUS GI MEDICAL TECHNOLOGIES LTD·05060513700045·(1) Oversleeve

EVIS LUCERA ELITE GASTROINTESTINAL VIDEOSCOPE

FDA Adverse Event
Injury ·AIZU OLYMPUS CO., LTD.·Product code FDS·March 27, 2023

INTRALASE FS2 LASER

FDA Adverse Event
Injury ·AMO MANUFACTURING USA LLC·Product code HNO·November 23, 2010

IOLMASTER

FDA Adverse Event
Injury ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·March 3, 2016

SINGLE USE ELECTROSURGICAL KNIFE

FDA Adverse Event
Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·March 27, 2023

ACUVUE OASYS

FDA Adverse Event
Injury ·JOHNSON & JOHNSON VISION CARE, INC. ¿ US·Product code LPM·June 6, 2019

Anti-Glutamate Receptor (Type Nmda) Ifa

FDA classification
FDA Class 2 ·Anti-Glutamate Receptor (Type Nmda) Ifa

FSK CO., LTD

FDA registration
FSK CO., LTD·1 product·🇰🇷 South Korea

DSK

FDA UDI
Shenzhen Urion Technology Co., Ltd·06953825905712·

ASK

FDA UDI
RELIANCE ORTHODONTIC PRODUCTS INC·D798ASKU0·The ASK Kit is intended for use to increase adh...

ASK

FDA UDI
RELIANCE ORTHODONTIC PRODUCTS INC·D798ASK0·The ASK, All surface bonding Kit is intended fo...

DSK

FDA UDI
Shenzhen Urion Technology Co., Ltd·06953825905705·

ALL SURFACE KIT

FDA UDI
RELIANCE ORTHODONTIC PRODUCTS INC·00840479200774·

MSK Precision Products, Inc.

FDA registration
MSK Precision Products, Inc.·5 products·🇺🇸 United States

Bershka BSK Espana S.A.

FDA registration
Bershka BSK Espana S.A.·1 product·🇪🇸 Spain

NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021;CSK-022; CSK-023; CSK-025

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ASK-300

FDA 510(k)
FDA Class 2 ·Cardiovascular

ASK System

FDA 510(k)
FDA Class 2 ·Orthopedic

ELIAN

FDA UDI
OSKO, INC.·00869126000413·Digital Diagnostic X-Ray System

Edge Air

FDA UDI
OSKO, INC.·00869126000444·Digital X-Ray flat panel detector used to acqui...