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FORCE FX ELECTROSURGICAL GENERATOR CS, 120 V

FDA Adverse Event
Injury ·COVIDIEN·Product code GEI·January 20, 2016

AIA-900

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code KHO·March 24, 2018

RIVA LC

FDA UDI
SDI LIMITED·DO3687009001·

RIVA PROTECT

FDA UDI
SDI LIMITED·DO3686809001·

AIA-2000

FDA Adverse Event
Malfunction ·TOSOH HI-TEC, INC.·Product code KHO·August 14, 2025

AIA-2000

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code KHO·March 15, 2018

RIVA BOND

FDA UDI
SDI LIMITED·DO3688006121·

RIVA LUTING

FDA UDI
SDI LIMITED·DO3686509001·

RIVA SILVER

FDA UDI
SDI LIMITED·DO3686709001·

RIVA LUTING

FDA UDI
SDI LIMITED·DO3686519001·

A1A-2000

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code KHO·April 6, 2018

Recorder, Attention Task Performance

FDA classification
FDA Unclassified ·Recorder, Attention Task Performance

LCD

FDA UDI
PARI RESPIRATORY EQUIPMENT, INC.·00744229220220·LC Disp. Neb Set, Ped. Mask

LCD

FDA UDI
PARI RESPIRATORY EQUIPMENT, INC.·00744229220183·LC Disp. Neb Set

LCD

FDA UDI
PARI RESPIRATORY EQUIPMENT, INC.·00744229220206·LC Disp. Neb Set, Adult Mask

LAD, MODEL LAD-01

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

LED SPA

FDA registration
LED SPA·1 product·🇮🇹 Italy

LAD (EPITURE EASYTOUCH), MODEL LAD-08

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

LLD CARE D.O.O.

FDA registration
LLD CARE D.O.O.·23 products·🇭🇷 Croatia

LED TECHNOLOGIES, INC.

FDA registration
LED TECHNOLOGIES, INC.·4 products·🇺🇸 United States