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Bodycap

US

Last updated May 30, 2026

What Bodycap makes

Bodycap manufactures a range of medical devices, including continuous electronic patient thermometers that are battery-powered, as well as medical monitors and systems such as the e-Viewer Medical monitor and the e-Celsius Medical System. Their products also include the Activator Medical and the e-Celsius Medical pill. These devices are designed to provide various medical monitoring and therapeutic functions.

The company's portfolio is regulated as Class II devices and is listed in the FDA's 510(k) and UDI registries. Bodycap is based in the US, where these regulatory listings are maintained. The company's devices are subject to the oversight of the FDA, ensuring compliance with relevant medical device regulations.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What type of products does Bodycap manufacture?

Bodycap makes medical devices like continuous electronic patient thermometers and medical monitors, because these are listed as examples of their products.

Where is Bodycap based?

Bodycap is based in the US, as indicated by its listing in US regulatory registries.

Which registries list Bodycap devices?

Bodycap devices are listed in the FDA's 510(k) and UDI registries, because these are the registries mentioned in the company's summary.

How are Bodycap devices classified?

Bodycap devices are classified as Class II, because this classification is specified for their products.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
bodycap.io
LinkedIn
—
Facebook
—
Phone
+33(0)261530329
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
263625724

Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
e-Viewer Medical monitor P040-M_FCC
FDA UDI
Class IIActive
Activator Medical P030-M
FDA UDI
Class IIActive
e-Celsius Medical System P072
FDA UDI
Class IIActive
e-Celsius Medical pill P024-M
FDA UDI
Class IIActive
e-Celsius Medical System K210924
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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Authorities

Not available yet.

FDA Establishments (1)

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

  • Bodycap Herouville Saint-Clair Calvados · FR FEI 3014271659