# Lumiscope Co., Inc.

- Location (FDA's records): Edison, NJ
- FDA decisions: 13 (1988–2003): 13 510(k) clearances
- Product codes: GZJ (3), FLL (2), ILY (1), FNM (1), CAF (1), LIH (1), BTI (1), GXY (1), DRT (1), IPF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Newlife Sciences, LLC: 1 (https://510kreport.com/company/newlife-sciences)
- Actherm, Inc.: 1 (https://510kreport.com/company/actherm)
- Shining World Health Care Co., Ltd.: 1 (https://510kreport.com/company/shining-world-health-care)
- Mediphysics Pain Centers of America: 1 (https://510kreport.com/company/mediphysics-pain-centers-of-america)

## Its most-cited devices
- K894127: Lumiscope Model 1000/Apcc Model 1000 (1989), cited by 2
- K954792: Lumiscope Model 2018 Thermometer (1996), cited by 1
- K924081: Lumisonic (1992), cited by 1

## Recent decisions
- K032714: Cardicare Model MT-301F & MT-301C (Oct 22, 2003)
- K954792: Lumiscope Model 2018 Thermometer (Jun 21, 1996)
- K931768: Interferential Current Therapy Unit (Feb 23, 1994)
- K925054: Infrared Lamp (Jun 29, 1993)
- K924081: Lumisonic (Nov 9, 1992)
- K920099: Gymman (Mar 9, 1992)
- K901849: Lumiscope Ems 8000 (Aug 24, 1990)
- K901096: Lumiscope Alternating Pressure Pad & Pump (Aug 21, 1990)

Source page: https://510kreport.com/company/lumiscope