Data / Medical devices / United States / Foreseeson Custom Displays, Inc.
Foreseeson Custom Displays, Inc.: FDA-registered device maker in Anaheim, CA, United States, 8 510(k) clearances
Foreseeson Custom Displays, Inc. is registered with the FDA (registration 3006615210) in Anaheim, CA, United States. It lists 4 device types. The FDA files 8 510(k) clearances under its listings, the newest dated October 31, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006615210
- Address
- 2210 E Winston RD, Anaheim, CA, United States, 92806
- Owner or operator
- FORESEESON CUSTOM DISPLAYS, INC. (10036004)
- Roles
- Complaint file establishment, Manufacturer, Remanufacturer, Repackager or relabeler
- First device listed
- April 12, 2011
- Registered through
- 2026
- Brand names listed
- CL24N, CW120N, CW60N, CX20N(CX20PUX), CX30N(CX30PQX), CX50N(CX50YQS), FM-A2701D(S), FM-A5502DC and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Camera, Surgical And Accessories | KQM | 1 | Complaint file establishment, Manufacturer, Remanufacturer, Repackager or relabeler | accessdata.fda.gov |
| Display, Diagnostic Radiology | PGY | 2 | Complaint file establishment, Remanufacturer | accessdata.fda.gov |
| Medical Device Data System | OUG | 1 | Complaint file establishment, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| System, Digital Image Communications, Radiological | LMD | 1 | Complaint file establishment, Manufacturer, Remanufacturer, Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 31, 2022 | K222722 | CW60N | PGY | Substantially Equivalent | Wide Corporation | accessdata.fda.gov |
| October 31, 2022 | K222717 | CL24N | PGY | Substantially Equivalent | Wide Corporation | accessdata.fda.gov |
| April 14, 2021 | K210493 | CX30N (CX30PQX) | PGY | Substantially Equivalent | Wide Corporation | accessdata.fda.gov |
| April 8, 2021 | K210491 | CW120N | PGY | Substantially Equivalent | Wide Corporation | accessdata.fda.gov |
| March 31, 2017 | K170783 | CX50N(CX50YQS) | PGY | Substantially Equivalent | Wide Corporation | accessdata.fda.gov |
| April 22, 2016 | K160353 | MX50N(MX50YQS) | PGY | Substantially Equivalent | Wide Corporation | accessdata.fda.gov |
| April 14, 2016 | K160346 | MX30N(MX30TQS) | PGY | Substantially Equivalent | Wide Corporation | accessdata.fda.gov |
| April 7, 2016 | K160355 | CX20N(CX20PUX) | PGY | Substantially Equivalent | Wide Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Medical Device Data System
- All makers of System, Digital Image Communications, Radiological
- All makers of Display, Diagnostic Radiology
- All makers of Camera, Surgical And Accessories
Updated October 31, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.