Cleared Traditional

FREEPRINT? splintmaster

K232448 · Detax GmbH · Dental
Oct 2023
Decision
59d
Days
Risk

About This 510(k) Submission

K232448 is an FDA 510(k) clearance for the FREEPRINT? splintmaster, a Mouthguard, Prescription, submitted by Detax GmbH (Ettingen, DE). The FDA issued a Cleared decision on October 12, 2023, 59 days after receiving the submission on August 14, 2023. This device falls under the Dental review panel.

Submission Details

510(k) Number K232448 FDA.gov
FDA Decision Cleared SESE
Date Received August 14, 2023
Decision Date October 12, 2023
Days to Decision 59 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF

Device Classification

Product Code MQC — Mouthguard, Prescription
Device Class