FDA 510(k)

Luvis Chair (LC700C)

K-Number: K233921 · 2024-09-06

Decision Date2024-09-06

Product CodeKLC

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Luvis Chair (LC700C) is the device name listed in this FDA 510(k) record. The listed applicant is Dentis Co., Ltd.. It received FDA 510(k) clearance on 2024-09-06 under 510(k) number K233921. The device is classified under product code KLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Luvis Chair (LC700C)?

Luvis Chair (LC700C) is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Dentis Co., Ltd.. The 510(k) number is K233921.

When did Luvis Chair (LC700C) receive FDA 510(k) clearance?

Luvis Chair (LC700C) received FDA 510(k) clearance on 2024-09-06, under 510(k) number K233921.

Who is the listed applicant for Luvis Chair (LC700C)?

The FDA 510(k) record lists Dentis Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Luvis Chair (LC700C)?

The FDA product code for Luvis Chair (LC700C) is KLC.

Other records listing Dentis Co., Ltd. as applicant

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.

K253493Dentis SQ-SL AXEL Fixture K241065ChecQ (AC100)K241063s-Clean ScanHealing Abutment K240511Dentis s-Clean SQ-SL Fixture K233544MESHEET K230126Dentis s-Clean Regular Abutment

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Related Devices (Code: KLC)

K151987DCI Edge Dental Chair with Operative UnitDci

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.