Lamberts Dalston , Ltd.: FDA filings under this applicant name
FDA lists 0 510(k) clearances under the applicant name “Lamberts Dalston , Ltd.”, plus 1 PMA decision, across 1 product code in 1 review panel. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| LLQ | Cap, Cervical, Contraceptive | 1 | 0 |
Review panels
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P870062 | PMA | PRENTIF TM CAVITY RIM CERVICAL CAP | 1988-05-23 |
Recalls
openFDA lists no recalls under a recalling firm named Lamberts Dalston , Ltd..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Lamberts Dalston , Ltd.?
FDA lists 0 510(k) clearances under the applicant name “Lamberts Dalston , Ltd.”, plus 1 PMA decision, across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
Which FDA product codes appear under Lamberts Dalston , Ltd.?
The most frequent FDA product codes under this applicant name are LLQ (Cap, Cervical, Contraceptive, 1).
Next steps
- See all 0 Lamberts Dalston , Ltd. clearances with predicates and recalls
- Run predicate analysis for product code LLQ, Lamberts Dalston , Ltd.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.