Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Dental Pain Eraser

K-Number: K192429 · 2020-01-14

Decision Date2020-01-14
Product CodeLWM
DecisionSubstantially Equivalent

Device Summary

Dental Pain Eraser is a medical device manufactured by Synapse Dental. It received FDA 510(k) clearance on 2020-01-14 under approval number K192429. The device is classified under product code LWM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dental Pain Eraser?

Dental Pain Eraser is a medical device that received FDA 510(k) clearance on 2020-01-14. It is manufactured by Synapse Dental. The 510(k) number is K192429.

When was Dental Pain Eraser approved by the FDA?

Dental Pain Eraser received FDA 510(k) clearance on 2020-01-14, under approval number K192429.

What company makes Dental Pain Eraser?

Dental Pain Eraser is manufactured by Synapse Dental.

What is the FDA product code for Dental Pain Eraser?

The FDA product code for Dental Pain Eraser is LWM.

Other Devices by Synapse Dental

Related Devices (Code: LWM)

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.