CEMENTEK
Filler, Bone Void, Calcium Compound
TEKNIMED SA
The following data is part of a premarket notification filed by Teknimed Sa with the FDA for Cementek.
Pre-market Notification Details
| Device ID | K041493 |
| 510k Number | K041493 |
| Device Name: | CEMENTEK |
| Classification | Filler, Bone Void, Calcium Compound |
| Applicant | TEKNIMED SA 1001 OAKWOOD BLVD Round Rock, TX 78681 |
| Contact | J.d. Webb |
| Correspondent | J.d. Webb TEKNIMED SA 1001 OAKWOOD BLVD Round Rock, TX 78681 |
| Product Code | MQV |
| CFR Regulation Number | 888.3045 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-06-04 |
| Decision Date | 2004-08-19 |
| Summary: | summary |
Trademark Results [CEMENTEK]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CEMENTEK 90822790 not registered Live/Pending |
Hunter, Michael 2021-07-12 |
 CEMENTEK 75622287 not registered Dead/Abandoned |
TNEMEC COMPANY, INC. 1999-01-19 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.