510(k) K254286 ยท DZL Screw, Fixation, Intraosseous
Guided Bone Regeneration System
| Applicant | DentalMaster(Xiamen)Medical Technology Co., Ltd., Xiamen, CN |
| Decision | Substantially Equivalent, Aug 24, 2026 |
| Received | Dec 31, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K254286
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.