Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Rhino Health, Inc. · 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) |
|---|---|---|---|---|---|
| K223859 | Rhino Non-sterile Powder-Free Nitrile Exam Glove – Periwinkl | Rhino Health, Inc. | 2023-02-13 | 52 | 0 |
| K221082 | Rhino Non-Sterile, Powder-Free Nitrile Exam Gloves – Periwin | Rhino Health, Inc. | 2022-11-30 | 231 | 0 |
| K203236 | Rhino Health Non-Sterile, Powder-free Nitrile Exam Glove | Rhino Health, Inc. | 2021-08-16 | 286 | 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