Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Efratgo, Ltd. HI Tech Bio-Surgical — 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) |
|---|---|---|---|---|---|
| K083648 | GOTFRIED PHYSIOLOGICAL HIP (PH) NAIL | Efratgo, Ltd. HI Tech Bio-Surgical | 2009-05-14 | 156 | 0 |
| K043233 | GOTFRIED PHYSIOLOGICAL HIP (PH) NAIL | Efratgo, Ltd. HI Tech Bio-Surgical | 2005-02-01 | 71 | 0 |
| K983814 | GOTFRIED PERCUTANEOUS COMPRESSION PLATING SYSTEM | Efratgo, Ltd. HI Tech Bio-Surgical | 1999-01-14 | 78 | 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