# Teleemg, LLC

- Location (FDA's records): Los Angeles, CA
- FDA decisions: 5 (2016–2025): 5 510(k) clearances
- Product codes: OBP (3), QCI (2)
- 510(k) review time since 2016: median 192 days, against 73 for FDA's reviews in the same codes and years (1 of 5 faster)
- Predicates its devices cite: 9 (4 its own); citations of its devices by later devices: 8 (4 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
- Tonica Elektronik A/S: 4 (https://510kreport.com/company/tonica-elektronik-a-s)
- The Magstim Company, Ltd.: 1 (https://510kreport.com/company/magstim)

## Firms that cite its devices most
- The Magstim Company, Ltd.: 1 (https://510kreport.com/company/magstim)
- Tonica Elektronik A/S: 1 (https://510kreport.com/company/tonica-elektronik-a-s)
- Revital Lab, Inc.: 1 (https://510kreport.com/company/revital-lab)
- Remed Co., Ltd.: 1 (https://510kreport.com/company/remed)

## Its most-cited devices
- K173441: Neurosoft TMS (also CloudTMS) (2017), cited by 4
- K160309: Neurosoft TMS (2016), cited by 3
- K221129: CloudTMS for OCD (2023), cited by 1

## Recent decisions
- K250689: CloudTMS Edge (Sep 14, 2025)
- K233742: CloudTMS Edge for OCD (Dec 22, 2023)
- K221129: CloudTMS for OCD (Mar 10, 2023)
- K173441: Neurosoft TMS (also CloudTMS) (Dec 13, 2017)
- K160309: Neurosoft TMS (Dec 22, 2016)

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