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Obtech Medical Sàrl

Country not established

Devices
13

What Obtech Medical Sàrl makes

Obtech Medical Sàrl manufactures gastric calibration tubes, including the REALIZE GCT180 and GCT360 models, designed for medical procedures involving the stomach. These devices are intended to assist in the accurate measurement and dilation of the esophageal or gastric lumen during interventions.

The company’s portfolio is regulated under Class II medical devices in the United States, with products listed via the FDA’s 510(k) clearance process. The manufacturer is based in the US, adhering to applicable regulatory requirements for these device classifications.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue13

Newest first, rows 1-13 of 13

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  • Na RLZB32DT

    Withdrawn Registry: GUDID Class:—
  • Na RLZB32D1

    Withdrawn Registry: GUDID Class:—
  • N/A RGBRS1

    Withdrawn Registry: GUDID Class:I
  • N/A RGCT360

    Withdrawn Registry: GUDID Class:II
  • Na RLZB32DGT

    Withdrawn Registry: GUDID Class:—
  • Na RLZB32DG1

    Withdrawn Registry: GUDID Class:—
  • N/A RHUB50

    Withdrawn Registry: GUDID Class:I
  • N/A RHUB90

    Withdrawn Registry: GUDID Class:I
  • N/A RGCT180

    Withdrawn Registry: GUDID Class:II
  • Na RLZPT2

    Withdrawn Registry: GUDID Class:III
  • Na RLZB32

    Withdrawn Registry: GUDID Class:III
  • Na RLZB22T

    Withdrawn Registry: GUDID Class:—
  • Realize Gastric Calibration Tube, Models GCT180, GCT360 Ref K071764

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-13 of 13

Company details

DUNS number
486911852
Phone
+1(877)384-4266

Frequently asked questions

How many devices does Obtech Medical Sàrl have in the registry?

The registry currently lists 13 devices for Obtech Medical Sàrl. Devices recorded under merged duplicate company entries are counted once.

Which registries list Obtech Medical Sàrl's devices?

Among its 13 most recently registered devices, Obtech Medical Sàrl has devices listed in FDA 510(k) (1 device) and FDA GUDID (12 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Obtech Medical Sàrl's devices fall under?

Among its 13 most recently registered devices, the classes recorded for Obtech Medical Sàrl's devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Obtech Medical Sàrl in the registry?

The most recently registered devices listed for Obtech Medical Sàrl include NA RLZB32DT, NA RLZB32D1, N/A RGBRS1 and N/A RGCT360.

Generated automatically from registry data and not verified by a human reviewer.