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FDA 510(k)

GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray

K-Number: K231205 · 2023-08-22

ApplicantGurunanda, LLC
Decision Date2023-08-22
Product CodeLFD
DecisionSubstantially Equivalent

Device Summary

GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray is the device name listed in this FDA 510(k) record. The listed applicant is Gurunanda, LLC. It received FDA 510(k) clearance on 2023-08-22 under 510(k) number K231205. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray?

GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray is a medical device that received FDA 510(k) clearance on 2023-08-22. The listed applicant is Gurunanda, LLC. The 510(k) number is K231205.

When did GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray receive FDA 510(k) clearance?

GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray received FDA 510(k) clearance on 2023-08-22, under 510(k) number K231205.

Who is the listed applicant for GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray?

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

What is the FDA product code for GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray?

The FDA product code for GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray is LFD.

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.

NCT00540774Optical Sensor for Photodynamic Detection of Oral PathologyCOMPLETEDNCT05401201Dual-light Antibacterial Photodynamic Therapy as an Adjunctive Treatment to Corticosteroid Treatment in OLPCOMPLETEDNCT07041671Evaluation Viral RNA and Virus Infectivity in Exhaled Air Before and After Use of One Dose With ColdZyme Mouth SprayRECRUITINGNCT07506018MucoLock™ for Treatment of StomatitisRECRUITINGNCT07511335Dry Needling Versus Stabilization Splint Therapy in Bruxism Associated Myofascial Temporomandibular DisordersCOMPLETEDNCT07564843Theravex® for Burning Mouth SyndromeCOMPLETED

Related Devices (Code: LFD)

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.

K253778Allday Moisturizing RinseElevate Oral CareK250390CloSYS® Dry Mouth Sensitive Mouth RinseRowpar Pharmaceuticals, Inc.K240508Salivea Dry Mouth Moisturizing Gel (Dry Mouth Moisturizing Gel)Laclede, Inc.K234015Caphosol® Artifical Saliva (32 doses sachet box)Eusa Pharma (Uk) LimitedK202689Dentilube SprayOxy2plus, LLCK203567Oral-B Dry Mouth Oral RinseThe Procter & Gamble Company

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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