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BBig B.V.

US

Last updated May 23, 2026

What BBig B.V. makes

BBig B.V. manufactures spectacle frames designed for corrective and fashion eyewear. The devices are intended for general use in optical prescriptions and include various styles and materials for different visual needs and preferences.

The company’s products are classified as Class I medical devices under US regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. BBig B.V. operates from the United States.

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

Frequently asked questions

What types of medical devices does BBig B.V. manufacture?

BBig B.V. specializes in spectacle frames, which are designed for both corrective and fashion eyewear. These devices are intended for general use in optical prescriptions and come in various styles and materials to cater to different visual needs and aesthetic preferences.

Where is BBig B.V. based, and how does that affect its regulatory standing?

BBig B.V. is based in the United States. Since its devices are regulated under US medical device laws, their classification and compliance requirements follow FDA guidelines. The company’s location ensures its products meet US-specific regulatory standards.

How are BBig B.V.’s devices classified under US regulations, and why?

BBig B.V.’s spectacle frames are classified as Class I medical devices under US regulations. This classification is typically assigned to low-risk devices where general controls are sufficient to ensure safety and effectiveness, such as spectacle frames, which pose minimal risk to users.

Are BBig B.V.’s devices listed in any regulatory registries, and if so, which ones?

Yes, BBig B.V.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices in the US market, ensuring transparency and traceability for regulatory and market surveillance purposes.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
408104979

Catalogue (3664)

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DeviceModel / ReferenceRegistriesClassStatus
Bbig F30134092
FDA UDI
Class IActive
Bbig TL06145203
FDA UDI
Class IActive
Bbig TL20738350
FDA UDI
Class IActive
Bbig F21044362
FDA UDI
Class IActive
Bbig F0114393
FDA UDI
Class IActive
Bbig 420845202
FDA UDI
Class IActive
Bbig 60738H04
FDA UDI
Class IActive
Bbig FTM165
FDA UDI
Class IActive
Bbig TL4206116S
FDA UDI
Class IActive
Bbig F03137166
FDA UDI
Class IActive
Bbig F0524392
FDA UDI
Class IActive
Bbig 8024702
FDA UDI
Class IActive
Bbig 50344307
FDA UDI
Class IActive
Bbig 03944241
FDA UDI
Class IActive
Bbig 20444402
FDA UDI
Class IActive
Bbig TL4903472
FDA UDI
Class IActive
Bbig 60142H01
FDA UDI
Class IActive
Bbig 60538H04
FDA UDI
Class IActive
Bbig F06247203
FDA UDI
Class IActive
Bbig F0164295
FDA UDI
Class IActive
Bbig F00638113
FDA UDI
Class IActive
Bbig 22740411
FDA UDI
Class IActive
Bbig 21944390
FDA UDI
Class IActive
Bbig TL40015141
FDA UDI
Class IActive
Bbig FTM92
FDA UDI
Class IActive
Bbig F22247427
FDA UDI
Class IActive
Bbig 0184195
FDA UDI
Class IActive
Bbig TL60247H07
FDA UDI
Class IActive
Bbig F22738402
FDA UDI
Class IActive
Bbig 05147100
FDA UDI
Class IActive
Bbig 03137166
FDA UDI
Class IActive
Bbig TR4903478
FDA UDI
Class IActive
Bbig F0524396
FDA UDI
Class IActive
Bbig F22245386
FDA UDI
Class IActive
Bbig 06247205
FDA UDI
Class IActive
Bbig F21944371
FDA UDI
Class IActive
Bbig 02141105
FDA UDI
Class IActive
Bbig F22147425
FDA UDI
Class IActive
Bbig 50344915
FDA UDI
Class IActive
Bbig F22447396
FDA UDI
Class IActive
Bbig 420745207
FDA UDI
Class IActive
Bbig 21250368
FDA UDI
Class IActive
Bbig 70044216
FDA UDI
Class IActive
Bbig 02031166
FDA UDI
Class IActive
Bbig F320246425
FDA UDI
Class IActive
Bbig TR21133349
FDA UDI
Class IActive
Bbig 420637204
FDA UDI
Class IActive
Bbig TL22544382
FDA UDI
Class IActive
Bbig 4903454
FDA UDI
Class IActive
Bbig TL21348371
FDA UDI
Class IActive

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