The following data is part of a premarket notification filed by Hi-tec Implants with the FDA for Smooth Fit.
Device ID | K941575 |
510k Number | K941575 |
Device Name: | SMOOTH FIT |
Classification | Implant, Endosseous, Root-form |
Applicant | HI-TEC IMPLANTS 5 MASKIT STREET INDUSTRL.ZONE P.O. BOX 2022 Herzlia, IL 46722 |
Contact | Roy Leshem |
Correspondent | Roy Leshem HI-TEC IMPLANTS 5 MASKIT STREET INDUSTRL.ZONE P.O. BOX 2022 Herzlia, IL 46722 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-03-31 |
Decision Date | 1994-11-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() SMOOTH FIT 85754364 4557613 Live/Registered |
First Quality Products, Inc. 2012-10-15 |
![]() SMOOTH FIT 75638496 not registered Dead/Abandoned |
SARA LEE CORPORATION 1999-02-12 |
![]() SMOOTH FIT 74395270 not registered Dead/Abandoned |
Koret of California, Inc. 1993-05-26 |
![]() SMOOTH FIT 73525135 not registered Dead/Abandoned |
SHIRLEY OF ATLANTA, INC. 1985-03-04 |