# Kinetic Technology, Inc.

- Location (FDA's records): Pittsburgh, PA
- FDA decisions: 5 (1988–1992): 5 510(k) clearances
- Product codes: LXM (5)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K922695: Kinetic Technology Precision Adjustor Mod. Shlcp-5 (Sep 30, 1992)
- K922692: Kinetic Technology Pocket Precision Adjustor (Sep 30, 1992)
- K922693: Kinetic Technoogy Precision Adjustor Model Shlcp-1 (Sep 30, 1992)
- K922694: Kinetic Technology Precision Adustor Model Shlcp-4 (Sep 30, 1992)
- K870910: Precision Spinal Adjuster Model 115 (Apr 26, 1988)

Source page: https://510kreport.com/company/kinetic-technology