CONVERBASE

Resin, Denture, Relining, Repairing, Rebasing

WILDE-USA, INC.

The following data is part of a premarket notification filed by Wilde-usa, Inc. with the FDA for Converbase.

Pre-market Notification Details

Device IDK912990
510k NumberK912990
Device Name:CONVERBASE
ClassificationResin, Denture, Relining, Repairing, Rebasing
Applicant WILDE-USA, INC. P.O. BOX 4168 Naperville,  IL  60567
ContactRobert W Bauer
CorrespondentRobert W Bauer
WILDE-USA, INC. P.O. BOX 4168 Naperville,  IL  60567
Product CodeEBI  
CFR Regulation Number872.3760 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1991-07-08
Decision Date1992-03-25

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.