# Noetix, Inc.

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 3 (1987–1989): 3 510(k) clearances
- Product codes: HNY (1), HQC (1), KNW (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
- K893992: Noetix, Biopsy Needle (Sep 8, 1989)
- K881635: Noetix (R) Surgical Extraction (TM) System (Jul 1, 1988)
- K871365: Capsulectomer Cystotome (Apr 16, 1987)

Source page: https://510kreport.com/company/noetix