Skip to content

Sinovation (Beijing) Medical Technology Co., Ltd.

ChinaFDA applicant, unverified FDA

Devices
25
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Sinovation (Beijing) Medical Technology Co., Ltd. makes

Sinovation (Beijing) Medical Technology Co., Ltd. manufactures the Sinobot X1, a robotic-assisted surgical system designed for minimally invasive procedures in orthopedic and joint surgeries.

The Sinobot X1 is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue25

Newest first, rows 1-25 of 25

Search and filter all 25 devices
Skip device list
  • Na Gud-Cr-G

    None Registry: GUDID Class:II
  • Na Gud-Dbs-Ao

    None Registry: GUDID Class:II
  • Na Gud-Dbs-LP

    None Registry: GUDID Class:II
  • Na Tt-2.2-30

    None Registry: GUDID Class:II
  • Na Tt-2.2-70

    None Registry: GUDID Class:II
  • Na Tt-5.0-65

    None Registry: GUDID Class:II
  • Na Tt-2.5-70

    None Registry: GUDID Class:II
  • Na Tt-50-30D

    None Registry: GUDID Class:II
  • Na Tt-50-40D

    None Registry: GUDID Class:II
  • Na Tt-50-50D

    None Registry: GUDID Class:II
  • Na Tt-50-35D

    None Registry: GUDID Class:II
  • Na Prb-Cr-S

    None Registry: GUDID Class:II
  • Na Tt-50-45D

    None Registry: GUDID Class:II
  • Na Gd-12

    None Registry: GUDID Class:II
  • Na Sda-A30-1

    None Registry: GUDID Class:II
  • Na Sda-A21-3

    None Registry: GUDID Class:II
  • NA Sinobot X1

    None Registry: GUDID Class:II
  • Na 37100016

    Withdrawn Registry: GUDID Class:II
  • Na 37110003

    None Registry: GUDID Class:II
  • Na 37100008

    Withdrawn Registry: GUDID Class:II
  • Na 37100009

    Withdrawn Registry: GUDID Class:II
  • Na 37100003

    Withdrawn Registry: GUDID Class:II
  • Na 37100013

    Withdrawn Registry: GUDID Class:II
  • Na 37100005

    Withdrawn Registry: GUDID Class:II
  • Sinobot X1 Ref K220072

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

Rows 1-25 of 25

Company details

DUNS number
560671783

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Sinovation (Beijing) Medical Technology Co., Ltd Beijing · CN FEI 3027616024

Frequently asked questions

How many devices does Sinovation (Beijing) Medical Technology Co., Ltd. have in the registry?

The registry currently lists 25 devices for Sinovation (Beijing) Medical Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sinovation (Beijing) Medical Technology Co., Ltd.'s devices?

Among its 25 most recently registered devices, Sinovation (Beijing) Medical Technology Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (24 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Sinovation (Beijing) Medical Technology Co., Ltd.'s devices fall under?

Among its 25 most recently registered devices, the classes recorded for Sinovation (Beijing) Medical Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Sinovation (Beijing) Medical Technology Co., Ltd. in the registry?

The most recently registered devices listed for Sinovation (Beijing) Medical Technology Co., Ltd. include NA GUD-CR-G, NA GUD-DBS-AO, NA GUD-DBS-LP and NA TT-2.2-30.

Which FDA establishments are linked to Sinovation (Beijing) Medical Technology Co., Ltd.?

1 FDA establishment is linked to Sinovation (Beijing) Medical Technology Co., Ltd. in the registry; they are listed on the company page.

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