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FDA 510(k)

FLOSSIE TOOTHFLOSS

K-Number: K903712 · 1990-09-05

ApplicantFlossie, Inc.
Decision Date1990-09-05
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLOSSIE TOOTHFLOSS is the device name listed in this FDA 510(k) record. The listed applicant is Flossie, Inc.. It received FDA 510(k) clearance on 1990-09-05 under 510(k) number K903712. The device is classified under product code JES. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOSSIE TOOTHFLOSS?

FLOSSIE TOOTHFLOSS is a medical device that received FDA 510(k) clearance on 1990-09-05. The listed applicant is Flossie, Inc.. The 510(k) number is K903712.

When did FLOSSIE TOOTHFLOSS receive FDA 510(k) clearance?

FLOSSIE TOOTHFLOSS received FDA 510(k) clearance on 1990-09-05, under 510(k) number K903712.

Who is the listed applicant for FLOSSIE TOOTHFLOSS?

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

What is the FDA product code for FLOSSIE TOOTHFLOSS?

The FDA product code for FLOSSIE TOOTHFLOSS is JES.

Related Clinical Trials

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: JES)

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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