Cordcap
510(k) K091380
Cordcap is a medical device (FDA unclassified; FDA product code MVL, Cord, Retraction) made by Centrix, Inc., cleared under FDA 510(k) K091380 on 30 Jul 2009, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK091380 | Date30 Jul 2009 | StatusActive |
Official records
- FDA 510(k) database K091380
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MVL
- Device class
- U
- Advisory committee
- Unknown
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code MVL (Cord, Retraction).
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- KORLEX-GR GINGIVAL RETRACTION PASTE by Biotech One, Inc.
- GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord by KERR CORPORATION