# Mend Technologies, Inc.

- Location (FDA's records): Dallas, TX
- FDA decisions: 3 (1988–1993): 3 510(k) clearances
- Product codes: HEB (1), BWN (1), JEA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K924094: Mend Apc (Mar 30, 1993)
- K883867: Cervical Biopsy Instrument (Nov 29, 1988)
- K884558: Iop Adjustable Stirrup (Nov 17, 1988)

Source page: https://510kreport.com/company/mend-technologies
