# Tenex Health, Inc.

- Location (FDA's records): Lake Forest,, CA
- FDA decisions: 3 (2013–2018): 3 510(k) clearances
- Names in FDA's records: Tenex Health, Inc. (2); Tenex Health (1)
- Product codes: LFL (3)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Misonix, Inc.: 2 (https://510kreport.com/company/misonix)
- American Optisurgical, Inc.: 1 (https://510kreport.com/company/american-optisurgical)

## Firms that cite its devices most
- Trice Medical, Inc.: 1 (https://510kreport.com/company/trice-medical)
- Tendonova Corporation: 1 (https://510kreport.com/company/tendonova)

## Its most-cited devices
- K123640: TX1 Tissue Removal System (2013), cited by 1
- K181367: Tenex Health TX System with the TXP MicroTip (2018), cited by 1
- K153299: Tenex Health TX System (2016), cited by 1

## Recent decisions
- K181367: Tenex Health TX System with the TXP MicroTip (Aug 28, 2018)
- K153299: Tenex Health TX System (Mar 3, 2016)
- K123640: TX1 Tissue Removal System (Mar 20, 2013)

Source page: https://510kreport.com/company/tenex-health