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FDA 510(k)

LITE FIL II A

K-Number: K920892 · 1992-09-01

ApplicantShofu Dental Corp.
Decision Date1992-09-01
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LITE FIL II A is the device name listed in this FDA 510(k) record. The listed applicant is Shofu Dental Corp.. It received FDA 510(k) clearance on 1992-09-01 under 510(k) number K920892. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITE FIL II A?

LITE FIL II A is a medical device that received FDA 510(k) clearance on 1992-09-01. The listed applicant is Shofu Dental Corp.. The 510(k) number is K920892.

When did LITE FIL II A receive FDA 510(k) clearance?

LITE FIL II A received FDA 510(k) clearance on 1992-09-01, under 510(k) number K920892.

Who is the listed applicant for LITE FIL II A?

The FDA 510(k) record lists Shofu Dental Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LITE FIL II A?

The FDA product code for LITE FIL II A is EBF.

Other records listing Shofu Dental Corp. as applicant

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Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, Inc.

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.

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