Clear Future, Inc.: FDA clearances and approvals
Clear Future, Inc. 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 |
|---|---|---|---|
| MBU | Single-Use Internal Condom | 1 | 0 |
Review panels
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P080002 | PMA | FC2 FEMALE CONDOM | 2009-03-10 |
Recalls
openFDA lists no recalls under a recalling firm named Clear Future, Inc..
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 Clear Future, Inc. have?
Clear Future, Inc. has 0 FDA 510(k) clearances, plus 1 PMA decision, across 1 product code in 1 review panel.
What devices does Clear Future, Inc. make?
Its most frequent FDA product codes are MBU (Single-Use Internal Condom, 1).
Has Clear Future, Inc. had device recalls?
openFDA lists no recalls under a recalling firm name matching Clear Future, Inc. Related entities may recall under other names.
Next steps
- See all 0 Clear Future, Inc. clearances with predicates and recalls
- Run predicate analysis for product code MBU, Clear Future, Inc.'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.