Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Advanced Mechanical Technology, Inc. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
90 daysmedian FDA review time
90 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K883131 | BIOMECHANICS FORCE PLATFORM #LG6-4-1000 & 2000 | Advanced Mechanical Technology, Inc. | 1988-10-24 | 90 | 0 |
| K883130 | BIOMECHANICS FORCE PLATFORM/# OR6-5-1000 & 2000 | Advanced Mechanical Technology, Inc. | 1988-10-24 | 90 | 0 |
| K883129 | BIOMECHANICS FORCE PLATFORM/#OR 6-6-1000 & 2000 | Advanced Mechanical Technology, Inc. | 1988-10-24 | 90 | 0 |
| K883198 | BIOVEC BIOMECHANIC FORCE ANALYSIS SYSTEM | Advanced Mechanical Technology, Inc. | 1988-10-24 | 88 | 0 |
| K883127 | MULTI-CHANNEL STRAIN-GAGE AMPLIFIER & POWER SUPPLY | Advanced Mechanical Technology, Inc. | 1988-09-30 | 66 | 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