Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Mis - Implant Technologies , Ltd. — 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) |
|---|---|---|---|---|---|
| K103089 | SEVEN IMPLANTS; BIOCOM IMPLANTS; LANCE IMPLANTS | Mis - Implant Technologies , Ltd. | 2011-09-15 | 331 | 0 |
| K080458 | MIS CREST WIDENER | Mis - Implant Technologies , Ltd. | 2008-12-17 | 301 | 0 |
| K040807 | MIS DENTAL IMPLANT SYSTEM | Mis - Implant Technologies , Ltd. | 2004-06-09 | 72 | 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