Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Tpc Advanced Technology, Inc. · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K071485 | TPC ADVANCECAM INTRA ORAL CAMERA SYSTEM, MODEL AIC 888 | Tpc Advanced Technology, Inc. | 2007-08-28 | 90 | 0 |
| K051547 | POWERMAX 25, MODEL PM25; POWERMAX 30, MODEL PM30 | Tpc Advanced Technology, Inc. | 2005-07-14 | 31 | 0 |
| K983029 | POWER PLUS 25K MODEL, S1000, POWER PLUS 30K MODEL,S1001 | Tpc Advanced Technology, Inc. | 1999-01-29 | 151 | 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