# Mednet Locator, Inc.

- Location (FDA's records): Memphis, TN
- FDA decisions: 9 (1997–2000): 9 510(k) clearances
- Product codes: ETD (3), ETA (3), ETB (2), ERL (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
- K001406: HA/Gold Total and Partial, Regular and Offset, Ossicular Replacement Prostheses (Aug 8, 2000)
- K001404: Gold Total and Partial, Regular and Offset, Ossicular Replacement Prostheses, Gold Total with Fountian Head, Gold Piston (Aug 8, 2000)
- K974174: Ultrabur (Mar 10, 1998)
- K972737: Causse Piston (Sep 5, 1997)
- K972735: Total Ossicular Replacement Prosthesis (Torp) (Sep 5, 1997)
- K972734: Partial Ossicular Replacement Prosthesis (Porp) (Sep 5, 1997)
- K972126: Myringotomy Tube (Jul 29, 1997)
- K971943: Myringotomy Tube (Jul 23, 1997)

Source page: https://510kreport.com/company/mednet-locator