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Shenzhen Borria Technology Co., Ltd.

ChinaFDA applicant, unverified FDA

Devices
8
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Shenzhen Borria Technology Co., Ltd. makes

Shenzhen Borria Technology Co., Ltd. manufactures LED therapy masks, including models MN1 and M226, designed for skin treatment and rejuvenation. The company also produces IPL (Intense Pulsed Light) devices for hair removal, available as handheld units and larger machines.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue8

Newest first, rows 1-8 of 8

  • Iborria BR2020

    None Registry: GUDID Class:II
  • Iborria M226

    None Registry: GUDID Class:II
  • Iborria BR223

    None Registry: GUDID Class:II
  • Iborria BR225

    None Registry: GUDID Class:II
  • Iborria MN1

    None Registry: GUDID Class:II
  • LED Therapy Mask (MN1, M226) Ref K242385

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • IPL Hair Removal Device Ref K232939

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • IPL hair removal machine Ref K213020

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

Company details

DUNS number
715959366
Phone
+86075583167375

FDA establishments1

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

  • Shenzhen Borria Technology Co., Ltd Shenzhen Guangdong · CN FEI 3021599225

Frequently asked questions

How many devices does Shenzhen Borria Technology Co., Ltd. have in the registry?

The registry currently lists 8 devices for Shenzhen Borria Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shenzhen Borria Technology Co., Ltd.'s devices?

Among its 8 most recently registered devices, Shenzhen Borria Technology Co., Ltd. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Shenzhen Borria Technology Co., Ltd.'s devices fall under?

Among its 8 most recently registered devices, the classes recorded for Shenzhen Borria Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Shenzhen Borria Technology Co., Ltd. in the registry?

The most recently registered devices listed for Shenzhen Borria Technology Co., Ltd. include IBORRIA BR2020, IBORRIA M226, IBORRIA BR223 and IBORRIA BR225.

Which FDA establishments are linked to Shenzhen Borria Technology Co., Ltd.?

1 FDA establishment is linked to Shenzhen Borria 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.