# Escreen, Inc.

> Medical device manufacturer record on deviCERTS, compiled from public registries. Escreen, Inc. is a medical device manufacturer, with 17 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/escreen-inc>
- Country: not established
- Role: Manufacturer
- DUNS: 014079359

## Figures

- Devices: 17
- FDA recalls (matched to the firm by name): 0

## Registry facts

*Every device of the manufacturer. A device listed in two registries counts in both.*

- Registries: FDA GUDID 16, FDA 510(k) 1
- Device classes: FDA Class II 13, FDA Class I 4

## Devices

The first 17 of 17, in the order of the canonical page, which lists them all.

- [eCUP™ E&I eCUP™](https://devicerts.com/devices/ecup-206) · Class II · GUDID · status: Listed
- [eREADER™ E&I V3 - Serviced](https://devicerts.com/devices/ereader-2090000003) · Class I · GUDID · status: Listed
- [eScreen eReader V3](https://devicerts.com/devices/escreen-ereader-207-209-adb1cc0c) · Class II · GUDID · status: Listed
- [eScreen eCup](https://devicerts.com/devices/escreen-ecup-201) · Class II · GUDID · status: Listed
- [eREADER™ E&I V3 - New](https://devicerts.com/devices/ereader-2070000003) · Class I · GUDID · status: Listed
- [mCup® MCP10A-001](https://devicerts.com/devices/mcup-r-mcp10a-001) · Class II · GUDID · status: Listed
- [eScreen eReader V4](https://devicerts.com/devices/escreen-ereader-207-209) · Class II · GUDID · status: Listed
- [xCupTM DUE-1117X-071-01](https://devicerts.com/devices/xcuptm-due-1117x-071-01) · Class II · GUDID · status: Listed
- [eREADER™ E&I V4 - New](https://devicerts.com/devices/ereader-2070000004) · Class I · GUDID · status: Listed
- [eREADER™ E&I V4 - Serviced](https://devicerts.com/devices/ereader-2090000004) · Class I · GUDID · status: Listed
- [xReader System BS-0610S](https://devicerts.com/devices/xreader-system-301) · Class II · GUDID · status: Active
- [mCup® MCP9A-001](https://devicerts.com/devices/mcup-r-mcp9a-001) · Class II · GUDID · status: Listed
- [mCup® MCP11A-001](https://devicerts.com/devices/mcup-r-mcp11a-001) · Class II · GUDID · status: Listed
- [mCup® MCP7A-001](https://devicerts.com/devices/mcup-r-mcp7a-001) · Class II · GUDID · status: Listed
- [mCup® MCP5A-001](https://devicerts.com/devices/mcup-r-mcp5a-001) · Class II · GUDID · status: Listed
- [mCup® MCP5-001](https://devicerts.com/devices/mcup-r-mcp5-001) · Class II · GUDID · status: Withdrawn
- [Escreen System](https://devicerts.com/devices/escreen-system-laf) · ref K003352 · Class II · 510(k) · status: Active · decision 2001-03-20

## Source and citation

- Cite as: Escreen, Inc. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/escreen-inc (data as of 2026-11-15).
- Data sources: [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA 510(k)](https://open.fda.gov/apis/device/510k/)
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/escreen-inc.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/manufacturers/escreen-inc
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.