Dental Pain Eraser

FDA 510(k) K182947 · Synapse Dental, LLC

Substantially Equivalent

510(k) numberK182947

Submission

Device name
Dental Pain Eraser
Applicant
Synapse Dental, LLC
Cranston, RI, US
Received
October 23, 2018
Decision date
March 26, 2019
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LWM – Device, Electrical Dental Anesthesia
Device class
Unclassified

Other 510(k)s with product code LWM

510(k)DeviceApplicantDecision
K193570Dental Pain EraserLWM · Special Synapse Dental01/17/2020SE
K192429Dental Pain EraserLWM · Traditional Synapse Dental01/14/2020SE
K011001Team-Up TM Dental Electronic Anesthesia SystemLWM · Traditional Satelec06/07/2001SE
K9353043M Dental Electronic Anesthesia (Dea) System 8670LWM · Traditional 3M Company03/16/1994SE
K9350853M Dental Electrononic Anesthesia (DEA0 System 8670 Additional ApplicationsLWM · Traditional 3M Company01/26/1994SE
K9350823M Dental Electronic Anesthesia (Dea) System 8670 ModificationLWM · Traditional 3M Company01/26/1994SE
K915717CedetaLWM · Traditional D-W Intl.11/23/1992SE
K9201193M Dental Electronic Anesthesia SystemLWM · Traditional 3M Company05/22/1992SE
K910625UltracalmLWM · Traditional Sion Technology, Inc.05/15/1992SE
K902948Comfortron II (TENS)LWM · Traditional M. D. Products12/17/1990SE

More from M. D. Products

510(k)DeviceDecision
K193570Dental Pain EraserLWM · Special 01/17/2020SE
K192429Dental Pain EraserLWM · Traditional 01/14/2020SE

Questions and answers

When was Dental Pain Eraser cleared by the FDA?

Dental Pain Eraser (K182947) received a 510(k) decision of Substantially Equivalent on March 26, 2019, 154 days after the submission was received.

What is the product code of K182947?

The FDA product code is LWM – Device, Electrical Dental Anesthesia, a Unclassified device.