Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)
K-Number: K251544 · 2026-08-07
Device Summary
Frequently Asked Questions
What is the Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)?
Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0) is a medical device that received FDA 510(k) clearance on 2026-08-07. The listed applicant is Lakong Medical Devices Co., Ltd.. The 510(k) number is K251544.
When did Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0) receive FDA 510(k) clearance?
Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0) received FDA 510(k) clearance on 2026-08-07, under 510(k) number K251544.
Who is the listed applicant for Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)?
The FDA 510(k) record lists Lakong Medical Devices Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)?
The FDA product code for Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0) is EIA.
Related Devices (Code: EIA)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.