Home › Sprintray, Inc. › NightGuard Flex

NightGuard Flex

Sprintray, Inc. · Model SRI-0202015 · UDI-DI 00850039704062

KMY MQC Prescription

510(k) clearances

1,702

Adverse events

Recalls

114

Facilities

Description

Indicated for the fabrication of orthodontic and dental appliances such as mouthguards, nightguards, splints and repositioners. 3D scanned image of a patient's teeh

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.