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FDA 510(k)

SUPERFIL LIGHT & SUPERFIL BONDING SYSTEM

K-Number: K811427 · 1981-08-20

ApplicantHarry J. Bosworth Co.
Decision Date1981-08-20
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SUPERFIL LIGHT & SUPERFIL BONDING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Harry J. Bosworth Co.. It received FDA 510(k) clearance on 1981-08-20 under 510(k) number K811427. 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 SUPERFIL LIGHT & SUPERFIL BONDING SYSTEM?

SUPERFIL LIGHT & SUPERFIL BONDING SYSTEM is a medical device that received FDA 510(k) clearance on 1981-08-20. The listed applicant is Harry J. Bosworth Co.. The 510(k) number is K811427.

When did SUPERFIL LIGHT & SUPERFIL BONDING SYSTEM receive FDA 510(k) clearance?

SUPERFIL LIGHT & SUPERFIL BONDING SYSTEM received FDA 510(k) clearance on 1981-08-20, under 510(k) number K811427.

Who is the listed applicant for SUPERFIL LIGHT & SUPERFIL BONDING SYSTEM?

The FDA 510(k) record lists Harry J. Bosworth Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPERFIL LIGHT & SUPERFIL BONDING SYSTEM?

The FDA product code for SUPERFIL LIGHT & SUPERFIL BONDING SYSTEM is EBF.

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Other records listing Harry J. Bosworth Co. 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.

K103585BOSWORTH AEGIS LINER & RESTORATIVE MATERIAL W/ACPK100731BOSWORTH AIR POLISHERK061611BOSWORTH DENTIN RESINK051224BOSWORTH SEALK043170BOSWORTH BONDK040548AEGIS ORTHO LIGHT-CURED ORTHODONTIC ADHESIVE

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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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