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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 F8034112
FDA UDI
Class IActive
Bbig F320248425
FDA UDI
Class IActive
Bbig 03838241
FDA UDI
Class IActive
Bbig 03738230
FDA UDI
Class IActive
Bbig 01640173
FDA UDI
Class IActive
Bbig TR8034113
FDA UDI
Class IActive
Bbig 0014399
FDA UDI
Class IActive
Bbig TR40015176
FDA UDI
Class IActive
Bbig F21844381
FDA UDI
Class IActive
Bbig TR42033184
FDA UDI
Class IActive
Bbig TR20736353
FDA UDI
Class IActive
Bbig 22145402
FDA UDI
Class IActive
Bbig TR21133180
FDA UDI
Class IActive
Bbig F20741431
FDA UDI
Class IActive
Bbig TR06047205
FDA UDI
Class IActive
Bbig TR21548367
FDA UDI
Class IActive
Bbig TL21637382
FDA UDI
Class IActive
Bbig TR8024702
FDA UDI
Class IActive
Bbig TR50344307
FDA UDI
Class IActive
Bbig F20147337
FDA UDI
Class IActive
Bbig TL20838411
FDA UDI
Class IActive
Bbig 00143101
FDA UDI
Class IActive
Bbig TL60045H04
FDA UDI
Class IActive
Bbig F22546397
FDA UDI
Class IActive
Bbig 490246154
FDA UDI
Class IActive
Bbig 420147176
FDA UDI
Class IActive
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FDA UDI
Class IActive
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FDA UDI
Class IActive
Bbig 20738382
FDA UDI
Class IActive
Bbig 04046242
FDA UDI
Class IActive
Bbig 50344918
FDA UDI
Class IActive
Bbig F320341340
FDA UDI
Class IActive
Bbig 301539170
FDA UDI
Class IActive
Bbig F03238235
FDA UDI
Class IActive
Bbig F22938415
FDA UDI
Class IActive
Bbig F8043910
FDA UDI
Class IActive
Bbig F03135226
FDA UDI
Class IActive
Bbig F0164090
FDA UDI
Class IActive
Bbig 22447395
FDA UDI
Class IActive
Bbig TL22245426
FDA UDI
Class IActive
Bbig F20736428
FDA UDI
Class IActive
Bbig F420747208
FDA UDI
Class IActive
Bbig F21546409
FDA UDI
Class IActive
Bbig F02741105
FDA UDI
Class IActive
Bbig F0134293
FDA UDI
Class IActive
Bbig 21346373
FDA UDI
Class IActive
Bbig F06147174
FDA UDI
Class IActive
Bbig TL21133180
FDA UDI
Class IActive
Bbig 21548365
FDA UDI
Class IActive
Bbig TR22245401
FDA UDI
Class IActive

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