# Misten Medical Corp.

- Location (FDA's records): Germantown, TN
- FDA decisions: 4 (1995–1996): 4 510(k) clearances
- Product codes: ETD (1), ETB (1), ETA (1), 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
- K962163: Misten Medical Misten Medical Surgical Drill (Jul 25, 1996)
- K955616: Misten Medical Reuter Bobbin Style Vent Tube (Jan 17, 1996)
- K955613: Misten Medical Partial Ossicular Replacement Prosthesis (Dec 22, 1995)
- K955615: Misten Medical Total Ossicular Replacement Prosthesis (Dec 22, 1995)

Source page: https://510kreport.com/company/misten-medical