# Endo Motor

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

- Canonical page: <https://devicerts.com/devices/endo-motor-ekx>
- Manufacturer: [Foshan Cicada Dental Instrument Co., Ltd](https://devicerts.com/manufacturers/foshan-cicada-dental-instrument-coltd) (China)
- Device class: Class IIa (EU MDD); Class I (US FDA); Unclassified (US FDA)
- FDA product code: EKX, LQY
- EMDN: L159099 ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER
- GMDN: Remotely-driven surgical/dental system drive cable (37708)

## Registrations and authorizations

- **EUDAMED** · CE/MDD · European Union · Basic UDI-DI B-06974456210259 · UDI-DI 06974456210259 · registered 2026-05-29 · status: Active
- **GUDID** · GUDID listing · United States · UDI-DI 06974456210259 · listed 2024-08-09 · status: Listed (GUDID: in commercial distribution)
- **510(k)** · FDA 510(k) · United States · K192649 · decision 2021-03-12 · decision SESE · status: Active

## Recalls

No recall on record.

## Identity

- Trade name: Endo Motor [EUDAMED]; CICADA [FDA GUDID (AccessGUDID)]
- Generic name: Remotely-driven surgical/dental system drive cable [FDA GUDID (AccessGUDID)]
- Model / reference: T-Fine-II [EUDAMED, FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 06974456210259 [EUDAMED, FDA GUDID (AccessGUDID)]
- Basic UDI-DI: B-06974456210259 [EUDAMED]
- 510(k) Number: K192649 [FDA 510(k), FDA GUDID (AccessGUDID)]
- FDA product code: EKX [FDA 510(k), FDA GUDID (AccessGUDID)]; LQY [FDA GUDID (AccessGUDID)]
- EMDN code: L159099 [EUDAMED]
- GMDN term: Remotely-driven surgical/dental system drive cable (37708) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class IIa [EUDAMED]; Class I [FDA 510(k)]; U [FDA GUDID (AccessGUDID)]
- Regulation: 21 CFR Part 872.4200 [FDA 510(k), FDA GUDID (AccessGUDID)]
- EU registration type: Legacy device (under a directive) [EUDAMED]
- EU market of registration: Türkiye [EUDAMED]
- Advisory committee: Dental [FDA 510(k)]
- FDA decision: SESE [FDA 510(k)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Clinical & Handling

- Sterilisation method: Moist Heat or Steam Sterilization [FDA GUDID (AccessGUDID)]

## Properties

- Sterilise before use: No [EUDAMED]; Yes [FDA GUDID (AccessGUDID)]
- Reusable: Yes [EUDAMED]
- Lot / batch number: Yes [FDA GUDID (AccessGUDID)]
- Serial number: Yes [FDA GUDID (AccessGUDID)]
- Manufacturing date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Single use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Contains latex: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Reprocessed single-use device: No [EUDAMED]
- Incorporates a substance derived from human blood or plasma: No [EUDAMED]
- Contains human tissues or cells: No [EUDAMED]
- Contains animal tissues or cells: No [EUDAMED]
- Administering medicine: No [EUDAMED]
- Measuring function: No [EUDAMED]
- Incorporates a medicinal substance: No [EUDAMED]
- Prescription use: No [FDA GUDID (AccessGUDID)]
- Over-the-counter: 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)]
- Expiration date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: Endo Motor, Foshan Cicada Dental Instrument Co., Ltd. deviCERTS medical device catalogue. https://devicerts.com/devices/endo-motor-ekx (data as of 2026-11-15).
- Data sources: [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [EUDAMED](https://ec.europa.eu/tools/eudamed)
- Registry records last synced: 2026-11-08
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/endo-motor-ekx.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/endo-motor-ekx
- 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.