SureClip
Clip, Implantable
CONMED CORPORATION
The following data is part of a premarket notification filed by Conmed Corporation with the FDA for Sureclip.
Pre-market Notification Details
| Device ID | K150936 |
| 510k Number | K150936 |
| Device Name: | SureClip |
| Classification | Clip, Implantable |
| Applicant | CONMED CORPORATION 525 FRENCH ROAD Utica, NY 13502 |
| Contact | Anna D'lima |
| Correspondent | Lisa Anderson CONMED CORPORATION 525 FRENCH ROAD Utica, NY 13502 |
| Product Code | FZP |
| CFR Regulation Number | 878.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-04-07 |
| Decision Date | 2015-10-23 |
| Summary: | summary |
Trademark Results [SureClip]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SURECLIP 86783114 5162103 Live/Registered |
Micro-Tech Endoscopy USA, Inc. 2015-10-09 |
 SURECLIP 77339806 3559809 Live/Registered |
Quasar Services 2007-11-29 |
 SURECLIP 75319403 2223259 Dead/Cancelled |
ACCO BRANDS CORPORATION 1997-07-03 |
 SURECLIP 73812432 1583532 Dead/Cancelled |
SURE MEDICAL PRODUCTS 1989-07-14 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.