Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Poskom 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) |
|---|---|---|---|---|---|
| K253244 | AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mi | Poskom Co., Ltd. | 2026-02-23 | 147 | 0 |
| K250976 | Airbile-100 | Poskom Co., Ltd. | 2025-12-19 | 263 | 0 |
| K222896 | AirRay | Poskom Co., Ltd. | 2022-12-20 | 88 | 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