Elevate Moisturizing Spray

FDA 510(k) K150074 · Elevate Oral Care

Substantially Equivalent

510(k) numberK150074

Submission

Device name
Elevate Moisturizing Spray
Applicant
Elevate Oral Care
West Palm Beach, FL, US
Received
January 14, 2015
Decision date
June 19, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LFD – Saliva, Artificial
Device class
Unclassified

Other 510(k)s with product code LFD

510(k)DeviceApplicantDecision
K253778Allday Moisturizing RinseLFD · Traditional Elevate Oral Care02/27/2026SE
K250390CloSYS® Dry Mouth Sensitive Mouth RinseLFD · Traditional Rowpar Pharmaceuticals, Inc.05/19/2025SE
K240508Salivea Dry Mouth Moisturizing Gel (Dry Mouth Moisturizing Gel)LFD · Traditional Laclede, Inc.04/19/2024SE
K234015Caphosol® Artifical Saliva (32 doses sachet box)LFD · Traditional Eusa Pharma (Uk) Limited03/11/2024SE
K231205GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral SprayLFD · Traditional Gurunanda, LLC08/22/2023SE
K202689Dentilube SprayLFD · Traditional Oxy2plus, LLC09/03/2021SE
K203567Oral-B Dry Mouth Oral RinseLFD · Traditional The Procter & Gamble Company04/05/2021SE
K201277Oral-B Dry Mouth Oral RinseLFD · Traditional The Procter & Gamble Company09/02/2020SE
K181839CVS Health Dry Mouth Spray, OraLabs Dry Mouth SprayLFD · Traditional Oralabs, Inc.11/21/2019SE
K190144MucoPEGLFD · Traditional Sunbio, Inc.11/05/2019SE

More from Sunbio, Inc.

510(k)DeviceDecision
K253778Allday Moisturizing RinseLFD · Traditional 02/27/2026SE
K233768Papacarie DuoLBH · Traditional 07/18/2024SE
K222323Black DiamondPHR · Traditional 06/23/2023SE
K131376Smartcoat 2.5% Naf VarnishLBH · Traditional 08/27/2013SE

Questions and answers

When was Elevate Moisturizing Spray cleared by the FDA?

Elevate Moisturizing Spray (K150074) received a 510(k) decision of Substantially Equivalent on June 19, 2015, 156 days after the submission was received.

What is the product code of K150074?

The FDA product code is LFD – Saliva, Artificial, a Unclassified device.