NoCord
Material, Impression
CENTRIX, INC.
The following data is part of a premarket notification filed by Centrix, Inc. with the FDA for Nocord.
Pre-market Notification Details
| Device ID | K152826 |
| 510k Number | K152826 |
| Device Name: | NoCord |
| Classification | Material, Impression |
| Applicant | CENTRIX, INC. 770 RIVER ROAD Shelton, CT 06484 |
| Contact | Greg Moreau |
| Correspondent | Greg Moreau CENTRIX, INC. 770 RIVER ROAD Shelton, CT 06484 |
| Product Code | ELW |
| CFR Regulation Number | 872.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-09-29 |
| Decision Date | 2016-05-27 |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817051020815 | K152826 | 000 |
| 00817051020808 | K152826 | 000 |
| 00817051020785 | K152826 | 000 |
| 00817051020778 | K152826 | 000 |
| 00817051020761 | K152826 | 000 |
Trademark Results [NoCord]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NOCORD 86763562 5047199 Live/Registered |
Centrix, Inc. 2015-09-21 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.