Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Anhui Powerguard Technology Co., 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) |
|---|---|---|---|---|---|
| K233520 | Powder free, Non-sterile, Blue Nitrile Examination Gloves, T | Anhui Powerguard Technology Co., Ltd. | 2024-01-12 | 72 | 0 |
| K211860 | Powder Free Nitrile Patient Examination Gloves, Blue Color | Anhui Powerguard Technology Co., Ltd. | 2021-08-13 | 58 | 0 |
| K191292 | Powder Free Vinyl Patient Examination Gloves, Clear (non-col | Anhui Powerguard Technology Co., Ltd. | 2019-11-05 | 175 | 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