Raypex 6
by Dentsply International Inc.
510(k) K131907
Raypex 6 is a device classified as Unclassified made by Dentsply International Inc., cleared under FDA 510(k) K131907 on 31 Jan 2014, 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 | NumberK131907 | Date31 Jan 2014 | StatusActive |
Official records
- FDA 510(k) database K131907
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LQY
- FDA applicant
- Dentsply International, Inc.
- Device class
- U
- Advisory committee
- Unknown
- FDA decision
- SESE Substantially Equivalent
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