CLEARCORRECT

Aligner, Sequential

CLEARCORRECT, INC.

The following data is part of a premarket notification filed by Clearcorrect, Inc. with the FDA for Clearcorrect.

Pre-market Notification Details

• Device ID: K082556
• 510k Number: K082556
• Device Name: CLEARCORRECT
• Classification: Aligner, Sequential
• Applicant: CLEARCORRECT, INC. 220 RIVER ROAD Claremont, NH 03743
• Contact: William Greenrose
• Correspondent: William Greenrose; CLEARCORRECT, INC. 220 RIVER ROAD Claremont, NH 03743
• Product Code: NXC
• CFR Regulation Number: 872.5470 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2008-09-04
• Decision Date: 2009-02-06
• Summary: summary