Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Kinetic Technology, Inc. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
118 daysmedian FDA review time
418 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K922693 | KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1 | Kinetic Technology, Inc. | 1992-09-30 | 118 | 0 |
| K922694 | KINETIC TECHNOLOGY PRECISION ADUSTOR MODEL SHLCP-4 | Kinetic Technology, Inc. | 1992-09-30 | 118 | 0 |
| K922692 | KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR | Kinetic Technology, Inc. | 1992-09-30 | 118 | 0 |
| K922695 | KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5 | Kinetic Technology, Inc. | 1992-09-30 | 118 | 1 |
| K870910 | PRECISION SPINAL ADJUSTER MODEL 115 | Kinetic Technology, Inc. | 1988-04-26 | 418 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda