Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Porex Technologies Corp. of Georgia · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K960859 | MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES | Porex Technologies Corp. of Georgia | 1996-05-29 | 89 | 0 |
| K884884 | OSSICULAR PROSTHESIS: 8 PARTIAL, 3 TOTAL | Porex Technologies Corp. of Georgia | 1989-06-16 | 206 | 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