Euclid Vision Corporation: FDA clearances and approvals
Euclid Vision Corporation has 0 FDA 510(k) clearances, plus 1 PMA decision, across 1 product code in 1 review panel.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| NUU | Lens, Contact, Orthokeratology, Overnight | 1 | 0 |
Review panels
- Ophthalmic (1)
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P040029 | PMA | Euclid Orthokeratology (oprifocon A) Contact Lenses for Overnight Wear and Euclid Orthokeratology (tisilfocon A) Contact | 2004-09-29 |
Recalls
openFDA lists no recalls under a recalling firm named Euclid Vision Corporation.
Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.
Frequently asked questions
How many FDA 510(k) clearances does Euclid Vision Corporation have?
Euclid Vision Corporation has 0 FDA 510(k) clearances, plus 1 PMA decision, across 1 product code in 1 review panel.
What devices does Euclid Vision Corporation make?
Its most frequent FDA product codes are NUU (Lens, Contact, Orthokeratology, Overnight, 1).
Has Euclid Vision Corporation had device recalls?
openFDA lists no recalls under a recalling firm name matching Euclid Vision Corporation. Related entities may recall under other names.
Next steps
- See all 0 Euclid Vision Corporation clearances with predicates and recalls
- Run predicate analysis for product code NUU, Euclid Vision Corporation's most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.