# Glenroe Technologies

- Location (FDA's records): Bradenton, FL
- FDA decisions: 9 (1992–1998): 9 510(k) clearances
- Names in FDA's records: Glenroe Technologies (8); Glenroe Technologies, Inc. (1)
- Product codes: ECI (4), ECS (1), DYW (1), KMY (1), EGD (1), DYN (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
- K980053: Glenroe Chain (Feb 24, 1998)
- K945535: Glenroe Ortho-Sil (Jan 27, 1995)
- K924351: Glenroe Elastibite Stimulator (Jan 6, 1994)
- K932920: Glenroe Plastic Bracket (Aug 24, 1993)
- K931462: Glenroe Chain (Jul 22, 1993)
- K924140: Tuff Ties (Apr 27, 1993)
- K924139: Glenroe Ortho Seps (Apr 8, 1993)
- K924211: Ejector (Mar 31, 1993)

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