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US
Last updated May 23, 2026
What VIDCO, INC makes
VIDCO, INC manufactures centralized patient monitors and related display systems, including the VIDCO NewtViewer, VIDCO NetViewer, VIDCO MDP, MDP2000 MEDICAL DATA PROCESSOR, and various display drivers such as the 580CD, 580CDR, 516YT, 520 DISPLAY DRIVER- STATUS I, and 620CSR, as well as the SMDS460 SURGICAL MONITOR DISPLAY SYSTEM.
The company's devices are classified as Class II and are listed in the FDA 510(k) and FDA UDI registries. VIDCO, INC is based in the US.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does VIDCO, INC manufacture?
VIDCO, INC manufactures centralized patient monitors and related display systems, including the VIDCO NewtViewer, VIDCO NetViewer, VIDCO MDP, MDP2000 MEDICAL DATA PROCESSOR, various display drivers like the 580CD and 516YT, and the SMDS460 SURGICAL MONITOR DISPLAY SYSTEM.
Where is VIDCO, INC based?
VIDCO, INC is based in the United States, as indicated by the country designation in the device data.
Which regulatory registries list VIDCO, INC's devices?
VIDCO, INC's devices are listed in the FDA 510(k) and FDA UDI registries, which are the regulatory databases that track medical devices in the United States.
How are VIDCO, INC's devices classified?
VIDCO, INC's devices are classified as Class II, which means they are subject to general controls and special controls to ensure their safety and effectiveness, but are considered lower risk than Class III devices.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 068779370
Catalogue (11)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| VIDCO NewtViewer - VIDCO Protocol | MDP2040-0200 | FDA UDI | Class II | Active |
| VIDCO NetViewer | MDP2040-0100 | FDA UDI | Class II | Active |
| Vidco Mdp | MDP2040-0600RV | FDA UDI | Class II | Active |
| Vidco Mdp | MDP2020-0600 | FDA UDI | Class II | Active |
| Mdp2000 Medical Data Processor | K972880 | FDA 510(k) | Class II | Active |
| 580cd Display Driver | K926162 | FDA 510(k) | Class II | Active |
| 580cdr Display Driver | K934093 | FDA 510(k) | Class II | Active |
| 516yt Display Driver | K926219 | FDA 510(k) | Class II | Active |
| 520 Display Driver- Status I | K926298 | FDA 510(k) | Class II | Active |
| 620csr Display Driver | K932894 | FDA 510(k) | Class II | Active |
| Smds460 Surgical Monitor Display System | K890353 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Authorities
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
VIDCO, INC has one recall record initiated on 2015-11-08, which has been terminated. The reason given was that testing at customer site showed a Remote Patient Monitoring System MDP2040-0100 in a continuous trap condition, preventing system reset and reboot, with two customers reporting system freezing that required power reapplication to restart.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Nov 8, 2015 | Z-0582-2016 | — | terminated | Testing at customer site showed unit Remote Patient Monitoring System MDP2040-0100 in a continuous trap condition, not allowing system to reset and reboot. Two customers recently complained of the system freezing and it could only be restarted if the user re-applied power. |