# OsteoProbe

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

- Canonical page: <https://devicerts.com/devices/osteoprobe-op-100>
- Manufacturer: [Active Life Scientific, Inc.](https://devicerts.com/manufacturers/active-life-scientific-inc) (United States)
- Device class: Class IIa (EU MDR)
- EMDN: V0399 MEASUREMENT DEVICES - OTHER

## Registrations and authorizations

- **EUDAMED** · CE/MDR · European Union · Basic UDI-DI 00860001719369AW · UDI-DI 00860001719369 · registered 2025-12-02 · status: Active
- **510(k)** · FDA 510(k) · United States · K250216 · issued 2025-09-11 · status: Active
- **510(k)** · FDA 510(k) · United States · K221195 · issued 2022-06-28 · status: Active
- **De Novo** · FDA De Novo · United States · DEN210013 · issued 2021-08-19 · status: Active

## Recalls

No recall on record.

## Identity

- Model / reference: OP-100 [EUDAMED]

## Identifiers

- Primary DI / UDI-DI: 00860001719369 [EUDAMED]
- Basic UDI-DI: 00860001719369AW [EUDAMED]
- EMDN code: V0399 [EUDAMED]

## Classification

- Device class: Class IIa [EUDAMED]
- EU registration type: Standard device [EUDAMED]
- EU market of registration: Spain [EUDAMED]

## Properties

- Measuring function: Yes [EUDAMED]
- Supplied sterile: No [EUDAMED]
- Sterilise before use: No [EUDAMED]
- Implantable: No [EUDAMED]
- Reusable: No [EUDAMED]
- Contains latex: No [EUDAMED]
- Reprocessed single-use device: No [EUDAMED]
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): 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]
- Contains endocrine-disrupting substances: No [EUDAMED]
- Administering medicine: No [EUDAMED]
- Incorporates a medicinal substance: No [EUDAMED]

## Source and citation

- Cite as: OsteoProbe, Active Life Scientific, Inc. deviCERTS medical device catalogue. https://devicerts.com/devices/osteoprobe-op-100 (data as of 2026-11-14).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA 510(k)](https://open.fda.gov/apis/device/510k/)
- Registry records last synced: 2026-10-24
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/osteoprobe-op-100.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/osteoprobe-op-100
- 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.