# Foreo, Inc.

- Location (FDA's records): Las Vegas, NV
- FDA decisions: 11 (2016–2026): 11 510(k) clearances
- Product codes: OHS (3), NFO (3), PAY (2), OAP (1), OLP (1), OHT (1)
- 510(k) review time since 2016: median 106 days, against 97 for FDA's reviews in the same codes and years (4 of 10 faster)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 2 (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 whose devices it cites most
- Dongguan Lescolton Intelligent Electrical Appliance Co., Ltd.: 1 (https://510kreport.com/company/dongguan-lescolton-intelligent-electrical-appliance)
- Lexington International, LLC: 1 (https://510kreport.com/company/lexington-international)
- Li-Tek Electronic Technology Corporation: 1 (https://510kreport.com/company/li-tek-electronic-technology)
- Theragun, Inc.: 1 (https://510kreport.com/company/theragun)
- Carol Cole Company Dba Nuface: 1 (https://510kreport.com/company/carol-cole-company-dba-nuface)

## Firms that cite its devices most
- Shenzhen Rainbow Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-rainbow-technology)
- Kam Yuen Plastic Products, Ltd.: 1 (https://510kreport.com/company/kam-yuen-plastic-products)

## Its most-cited devices
- K241102: Luna 4 plus (2024), cited by 2

## Recent decisions
- K261565: Faq™ (Faq 411) (Oct 22, 2026)
- K253683: FAQ™ (LED Panel); FAQ™ (Dual LED Panel) (Feb 20, 2026)
- K242747: FAQ™ (302) (Dec 11, 2024)
- K241102: Luna 4 plus (Aug 20, 2024)
- K240616: FAQ™ (102) (Jul 15, 2024)
- K232242: BEAR 2 Body (May 13, 2024)
- K240378: Faq™ 201, Faq™ 202 (Apr 19, 2024)
- K231977: PEACH 2, PEACH 2 Duo, PEACH 2 go (Sep 25, 2023)

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