Nexus CMF, LLC: FDA clearances and approvals
Nexus CMF, LLC has 0 FDA 510(k) clearances, plus 2 PMA decisions, across 2 product codes in 1 review panel.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| LZD | Joint, Temporomandibular, Implant | 1 | 0 |
| MPI | Glenoid Fossa Prosthesis | 1 | 0 |
Review panels
- Dental (2)
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P000035 | PMA | TMJ FOSSA-EMINENCE PROSTHESIS(TM) | 2001-02-27 |
| P000023 | PMA | TMJ FOSSA-EMINENCE/CONDYLAR PROSTHESES | 2001-01-05 |
Recalls
openFDA lists no recalls under a recalling firm named Nexus CMF, LLC.
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 Nexus CMF, LLC have?
Nexus CMF, LLC has 0 FDA 510(k) clearances, plus 2 PMA decisions, across 2 product codes in 1 review panel.
What devices does Nexus CMF, LLC make?
Its most frequent FDA product codes are LZD (Joint, Temporomandibular, Implant, 1); MPI (Glenoid Fossa Prosthesis, 1).
Has Nexus CMF, LLC had device recalls?
openFDA lists no recalls under a recalling firm name matching Nexus CMF, LLC. Related entities may recall under other names.
Next steps
- See all 0 Nexus CMF, LLC clearances with predicates and recalls
- Run predicate analysis for product code LZD, Nexus CMF, LLC'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.