Digital Prism Correction Feature (DPCF)
510(k) K250143
Digital Prism Correction Feature (DPCF) is a Class I device made by Apple Inc., cleared under FDA 510(k) K250143 on 23 Jun 2025, active as of 11 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 | NumberK250143 | Date23 Jun 2025 | StatusActive |
Official records
- FDA 510(k) database K250143
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- SCW
- FDA applicant
- Apple, Inc.
- Device class
- Class I
- Regulation
- 21 CFR Part 886.1655
- Advisory committee
- Ophthalmic
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K250143
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| Digital Prism Correction Feature (DPCF) Feature version 1.X | Feature version 1.X | 00195949948411 | — | On the market |