Vilex IN Tennessee, Inc.
Vilex IN Tennessee, Inc. holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2019, with 3 FDA device recalls on record.
Top product codes for Vilex IN Tennessee, Inc.
FDA recalls by Vilex IN Tennessee, Inc.
- Z-1721-2015 — Vilex, Inc., FUZE 10.0 mm x 150 mm, Product # FZ100-150T-25. Ankle arthrodesis, tibio-talo-calcaneal arthrodesis.
- Z-1723-2015 — Vilex, Inc., FUZE 10.0 mm x 250 mm, Product # FZ100-250T-25. Ankle arthrodesis, tibio-talo-calcaneal arthrodesis.
- Z-1722-2015 — Vilex, Inc., FUZE 10.0 mm x 200 mm, Product # FZ100-200T-25. Ankle arthrodesis, tibio-talo-calcaneal arthrodesis.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Vilex IN Tennessee, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.