
Sprintray, Inc.
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NightGuard Flex is an FDA 510(k)-cleared medical device (K212448) manufactured by Sprintray, Inc.. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on November 11, 2021.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031