The following data is part of a premarket notification filed by Wieland Dental + Technik Gmbh & Co. Kg with the FDA for Allux.
Device ID | K050203 |
510k Number | K050203 |
Device Name: | ALLUX |
Classification | Powder, Porcelain |
Applicant | WIELAND DENTAL + TECHNIK GMBH & CO. KG SCHWENNINGER STRABE 13 Pforzheim, DE D-75179 |
Contact | Gerhard Polzer |
Correspondent | Gerhard Polzer WIELAND DENTAL + TECHNIK GMBH & CO. KG SCHWENNINGER STRABE 13 Pforzheim, DE D-75179 |
Product Code | EIH |
CFR Regulation Number | 872.6660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-01-28 |
Decision Date | 2005-02-14 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ALLUX 97225170 not registered Live/Pending |
Side, Inc. 2022-01-18 |
ALLUX 85797078 4769074 Live/Registered |
Nabtesco Corporation 2012-12-07 |
ALLUX 79014237 3159045 Dead/Cancelled |
Wieland Dental + Technik GmbH & Co. KG 2004-12-28 |
ALLUX 78562773 3276582 Dead/Cancelled |
ALLUX MEDICAL, INC. 2005-02-08 |
ALLUX 73191241 1144609 Dead/Cancelled |
Heinrich Odermath GmbH 1978-10-30 |