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FDA 510(k)

“FLNT Base” and “FLNT Temp”

K-Number: K253380 · 2026-03-02

Decision Date2026-03-02
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

“FLNT Base” and “FLNT Temp” is the device name listed in this FDA 510(k) record. The listed applicant is Liaoning Upcera Co., Ltd.. It received FDA 510(k) clearance on 2026-03-02 under 510(k) number K253380. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the “FLNT Base” and “FLNT Temp”?

“FLNT Base” and “FLNT Temp” is a medical device that received FDA 510(k) clearance on 2026-03-02. The listed applicant is Liaoning Upcera Co., Ltd.. The 510(k) number is K253380.

When did “FLNT Base” and “FLNT Temp” receive FDA 510(k) clearance?

“FLNT Base” and “FLNT Temp” received FDA 510(k) clearance on 2026-03-02, under 510(k) number K253380.

Who is the listed applicant for “FLNT Base” and “FLNT Temp”?

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

What is the FDA product code for “FLNT Base” and “FLNT Temp”?

The FDA product code for “FLNT Base” and “FLNT Temp” is EBG.

Other records listing Liaoning Upcera 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.

Related Devices (Code: EBG)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.