Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Sharplan Industries, Inc. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K861044 | MODEL 2100 ND:YAG SURGICAL LASER NEUROSURGICAL IND | Sharplan Industries, Inc. | 1986-10-28 | 224 | 0 |
| K861047 | MODEL 2100 ND:YAG SURGICAL LASER GASTROINTESTINAL | Sharplan Industries, Inc. | 1986-06-17 | 91 | 0 |
| K861046 | MODEL 2100 ND:YAG SURGICAL LASER UROLOGICAL INDICA | Sharplan Industries, Inc. | 1986-05-02 | 45 | 0 |
| K861045 | MODEL 2100 ND:YAG SURGICAL LASER PULMONARY INDICAT | Sharplan Industries, Inc. | 1986-04-23 | 36 | 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