510(k) K072768 ยท DZE Implant, Endosseous, Root-Form
RESTORE, STAGE-1, RENOVA PRIMASOLO AND PRIMACONNEX DENTAL IMPLANTS
| Applicant | Lifecore Biomedical, Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Oct 23, 2007 |
| Received | Sep 28, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072768
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 16, 2017 | Keystone Dental Inc STAGE-1 RDS COC Abutment Plastic Sleeve, Non-Lock, Multi-Unit; Catalog Number: S2437-01-1K Terminated |
DZE | None listed |
| Aug 25, 2017 | Keystone Dental Inc Stage-1 RDS Indexed Abutment for RDS Stage-1 Single Stage
Implants
Keystone s implants are intended for use in partially or fully edentulous mandibles and maxillae, in support of single or multip Terminated |
DZE | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.