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IODINE LEVEL 3

FDA UDI
UTAK LABORATORIES, INC.·B800IOD3SFSQ0·IODINE LEVEL 3

IODINE LEVEL 2

FDA UDI
UTAK LABORATORIES, INC.·B800IOD2SFSQ0·IODINE LEVEL 2

IODINE LEVEL 1

FDA UDI
UTAK LABORATORIES, INC.·B800IOD1SFSQ0·IODINE LEVEL 1

ILED-7

FDA Adverse Event
Injury ·TRUMPF MEDICAL SYSTEMS·Product code FSQ·December 21, 2017

KNIFE LIGHT 10/PK

FDA Adverse Event
Malfunction ·STRYKER OSTEOSYNTHESIS-FREIBURG·Product code FSQ·June 3, 2013

SATIN SLIP

FDA Adverse Event
Malfunction ·RESPIRATORY·Product code FSQ·September 29, 2004

KNIFE LIGHT 10/PK

FDA Adverse Event
Malfunction ·STRYKER OSTEOSYNTHESIS-FREIBURG·Product code FSQ·May 8, 2013

ILED7

FDA Adverse Event
Malfunction ·TRUMPF MEDIZIN SYSTEME GMBH + CO. KG·Product code FSQ·November 20, 2018

ILED7 SURGICAL LIGHT

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code FSQ·August 26, 2025

TRULIGHT DUO

FDA Adverse Event
Malfunction ·TRUMPF MEDIZIN SYSTEME GMBH + CO. KG·Product code FSQ·August 16, 2018

LIGHT SOURCE

FDA Adverse Event
Malfunction ·Product code FSQ·April 27, 2023

PALOMAR MEDILUX

FDA Adverse Event
Injury ·PALOMAR MEDICAL TECHNOLOGIES·Product code FSQ·October 5, 2004

ILED 7 SURGICAL LIGHTS

FDA Adverse Event
Injury ·BAXTER MEDICAL SYSTEMS GMBH + CO. KG·Product code FSQ·March 13, 2025

Light, Surgical, Instrument

FDA classification
FDA Class 2 ·Light, Surgical, Instrument

FSK CO., LTD

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

FAQ™ 201, FAQ™ 202

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

FSN Medical korea inc.

FDA registration
FSN Medical korea inc.·1 product·🇰🇷 South Korea

NANJING FSN MEDICAL CO.LTD.

FDA registration
NANJING FSN MEDICAL CO.LTD.·1 product·🇨🇳 China

NATIONAL DISTRIBUTION & CONTRACTING INC.

FDA UDI
NORDENT MANUFACTURING INC·00840018601680·CONDNSER #0/1 SERR QUALA

FAQ™ (LED Panel); FAQ™ (Dual LED Panel)

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