Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Seirin-America, 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) |
|---|---|---|---|---|---|
| K970260 | SEIRIN JR ACUPUNCTURE NEEDLES | Seirin-America, Inc. | 1997-02-10 | 18 | 0 |
| K970254 | SEIRIN PYONEX ACUPUNCTURE NEEDLES | Seirin-America, Inc. | 1997-02-10 | 19 | 0 |
| K963769 | SEIRIN SPINEX INTRADERMAL ACUPUNCTURE NEEDLES | Seirin-America, Inc. | 1996-10-16 | 27 | 0 |
| K962809 | SEIRIN ACUPUNCTURE NEEDLES | Seirin-America, Inc. | 1996-08-16 | 29 | 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