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FDA 510(k)

POWDERLITE

K-Number: K760369 · 1976-08-11

ApplicantThe S. S. White Co.
Decision Date1976-08-11
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

POWDERLITE is the device name listed in this FDA 510(k) record. The listed applicant is The S. S. White Co.. It received FDA 510(k) clearance on 1976-08-11 under 510(k) number K760369. 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 POWDERLITE?

POWDERLITE is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is The S. S. White Co.. The 510(k) number is K760369.

When did POWDERLITE receive FDA 510(k) clearance?

POWDERLITE received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760369.

Who is the listed applicant for POWDERLITE?

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

What is the FDA product code for POWDERLITE?

The FDA product code for POWDERLITE is EBF.

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Other records listing The S. S. White 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.

K852745PORCELAIN VENEER SYSTEM BONDING KITK852744CHARACTERIZER KIT VISIBLE LIGHT CURED RESTOR-COLORK853005S.S. WHITE DENTAL X-RAY FILM HOLDER & ALIGNING ARMK852743PORCELAIN VENEER SYSTEM LABORATORY KITK852182EASY TRAY & EASY BASE CUSTOM IMPRESSION TRAY MATERK837440UNKNOWN

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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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