K251544
- 510(k) number
- K251544
- Device name
- Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)
- Applicant
- Lakong Medical Devices Co., Ltd. CN
- Product code
- EIA — Unit, Operative Dental
- Decision date
- 2026-08-07
- Date received
- 2025-05-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K251544
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.