FDA 510(k)

Oral-B Dry Mouth Oral Rinse

K-Number: K203567 · 2021-04-05

Decision Date2021-04-05

Product CodeLFD

DecisionSubstantially Equivalent

Device Summary

Oral-B Dry Mouth Oral Rinse is a medical device manufactured by The Procter & Gamble Company. It received FDA 510(k) clearance on 2021-04-05 under approval number K203567. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Oral-B Dry Mouth Oral Rinse?

Oral-B Dry Mouth Oral Rinse is a medical device that received FDA 510(k) clearance on 2021-04-05. It is manufactured by The Procter & Gamble Company. The 510(k) number is K203567.

When was Oral-B Dry Mouth Oral Rinse approved by the FDA?

Oral-B Dry Mouth Oral Rinse received FDA 510(k) clearance on 2021-04-05, under approval number K203567.

What company makes Oral-B Dry Mouth Oral Rinse?

Oral-B Dry Mouth Oral Rinse is manufactured by The Procter & Gamble Company.

What is the FDA product code for Oral-B Dry Mouth Oral Rinse?

The FDA product code for Oral-B Dry Mouth Oral Rinse is LFD.

Related Clinical Trials

NCT05401201 Dual-light Antibacterial Photodynamic Therapy as an Adjunctive Treatment to Corticosteroid Treatment in OLP COMPLETED

Other Devices by The Procter & Gamble Company

K201277Oral-B Dry Mouth Oral Rinse K200881Oral-B iO Test Drive Power Brush Trial Program Kit

Related Devices (Code: LFD)

K163029Hydris Oral RinseBiopharm Consult, LLC K163476LubricityYou First Services, Incorporated K162167Caphosol Artifical Saliva TabletsEusa Pharma (Uk) Limited K180680Salivea Dry Mouth Mouthwash, Salivea Dry Mouth MouthsprayLaclede, Inc. K173808VoutiaJeffrey Ward Cash, Dds K181134GUM HYDRAL Dry Mouth Oral Gel, GUM HYDRAL Dry Mouth Oral Rinse, GUM HYDRAL Dry Mouth Oral SpraySunstar Americas, Inc.

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.