# Revitive Medic Plus 3156AD

> Active: United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/revitive-medic-plus-3158>
- Manufacturer: [Actegy, Ltd.](https://devicerts.com/manufacturers/actegy-ltd) (FDA registration: United States)
- Device class: Class II (US FDA)
- FDA product code: NYN, IPF, GZJ, NUH, NGX
- GMDN: Analgesic transcutaneous electrical nerve stimulation system (35372)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 00858058005146 · listed 2019-10-09 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K190924 · decision 2019-07-05 · decision SESE · status: Active · from GUDID

## Recalls

No recall on record.

## Identity

- Trade name: Revitive Medic Plus [FDA GUDID (AccessGUDID)]
- Generic name: Analgesic transcutaneous electrical nerve stimulation system [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: 3156AD [FDA GUDID (AccessGUDID)]; 3158 [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 00858058005146 [FDA GUDID (AccessGUDID)]
- 510(k) Number: K190924 [FDA GUDID (AccessGUDID)]
- FDA product code: NYN [FDA GUDID (AccessGUDID)]; IPF [FDA GUDID (AccessGUDID)]; GZJ [FDA GUDID (AccessGUDID)]; NUH [FDA GUDID (AccessGUDID)]; NGX [FDA GUDID (AccessGUDID)]
- GMDN term: Analgesic transcutaneous electrical nerve stimulation system (35372) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 882.5890 [FDA GUDID (AccessGUDID)]; 890.5850 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Over-the-counter: Yes [FDA GUDID (AccessGUDID)]
- Serial number: Yes [FDA GUDID (AccessGUDID)]
- Manufacturing date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [FDA GUDID (AccessGUDID)]
- Sterilise before use: No [FDA GUDID (AccessGUDID)]
- Single use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Contains latex: No [FDA GUDID (AccessGUDID)]
- Prescription use: No [FDA GUDID (AccessGUDID)]
- Convenience kit: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Lot / batch number: No [FDA GUDID (AccessGUDID)]
- Expiration date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: Revitive Medic Plus 3156AD, Actegy, Ltd. deviCERTS medical device catalogue. https://devicerts.com/devices/revitive-medic-plus-3158 (data as of 2026-11-14).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/)
- Registry records last synced: 2026-10-22
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/revitive-medic-plus-3158.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/devices/revitive-medic-plus-3158
- 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.