# Scimage, Inc.

> Medical device manufacturer record on deviCERTS, compiled from public registries. Scimage, Inc. is a medical device manufacturer, with 4 devices listed in FDA 510(k) and FDA GUDID (FDA Class II and I) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/scimage-inc>
- Country: United States (FDA applicant, unverified)
- Role: Manufacturer
- Registrations: FDA
- FDA FEI: 3000206530
- DUNS: 958220790

## Figures

- Devices: 4
- 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 510(k) 3, FDA GUDID 1
- Device classes: FDA Class II 3, FDA Class I 1

## Devices

The first 4 of 4, in the order of the canonical page, which lists them all.

- [PicomEnterprise 3.x](https://devicerts.com/devices/picomenterprise-3-x) · Class II · GUDID · status: Active
- [Netra Workstation And Netramd Software](https://devicerts.com/devices/netra-workstation-and-netramd-software-llz) · ref K003484 · Class II · 510(k) · status: Active · decision 2001-01-19
- [Netra Workstation System & Netra Md Software](https://devicerts.com/devices/netra-workstation-system-and-netra-md-software-lmd) · ref K960911 · Class I · 510(k) · status: Active · decision 1996-05-29
- [Scimage Picomenterprise](https://devicerts.com/devices/scimage-picomenterprise-llz) · ref K073169 · Class II · 510(k) · status: Active · decision 2008-01-09

## Source and citation

- Cite as: Scimage, Inc. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/scimage-inc (data as of 2026-11-15).
- Data sources: [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA registration and listing](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/rl.cfm)
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/scimage-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/scimage-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.