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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 F420333226
FDA UDI
Class IActive
Bbig F490246102
FDA UDI
Class IActive
Bbig F420145145
FDA UDI
Class IActive
Bbig F22347408
FDA UDI
Class IActive
Bbig 60345H01
FDA UDI
Class IActive
Bbig 03942241
FDA UDI
Class IActive
Bbig FTM75
FDA UDI
Class IActive
Bbig TR32028343
FDA UDI
Class IActive
Bbig FM153676
FDA UDI
Class IActive
Bbig F0174295
FDA UDI
Class IActive
Bbig 02337174
FDA UDI
Class IActive
Bbig TR60247H06
FDA UDI
Class IActive
Bbig TR4205110
FDA UDI
Class IActive
Bbig 01642540
FDA UDI
Class IActive
Bbig 60043H03
FDA UDI
Class IActive
Bbig 06147540
FDA UDI
Class IActive
Bbig F30054491
FDA UDI
Class IActive
Bbig F0114392
FDA UDI
Class IActive
Bbig 420145141
FDA UDI
Class IActive
Bbig F23140371
FDA UDI
Class IActive
Bbig TR60740H04
FDA UDI
Class IActive
Bbig TR320246343
FDA UDI
Class IActive
Bbig TR23346380
FDA UDI
Class IActive
Bbig TL42087204
FDA UDI
Class IActive
Bbig F30134292
FDA UDI
Class IActive
Bbig 0193990
FDA UDI
Class IActive
Bbig F8024502
FDA UDI
Class IActive
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FDA UDI
Class IActive
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FDA UDI
Class IActive
Bbig 20248343
FDA UDI
Class IActive
Bbig 70144217
FDA UDI
Class IActive
Bbig 05048170
FDA UDI
Class IActive
Bbig 420246127
FDA UDI
Class IActive
Bbig TR50342307
FDA UDI
Class IActive
Bbig TM237
FDA UDI
Class IActive
Bbig F22147405
FDA UDI
Class IActive
Bbig F320246226
FDA UDI
Class IActive
Bbig 20736428
FDA UDI
Class IActive
Bbig TL22740381
FDA UDI
Class IActive
Bbig TL23346435
FDA UDI
Class IActive
Bbig F03038161
FDA UDI
Class IActive
Bbig F01340211
FDA UDI
Class IActive
Bbig TR8024502
FDA UDI
Class IActive
Bbig F02241164
FDA UDI
Class IActive
Bbig 22247431
FDA UDI
Class IActive
Bbig TR23140436
FDA UDI
Class IActive
Bbig F22145402
FDA UDI
Class IActive
Bbig TL21548409
FDA UDI
Class IActive
Bbig TR320248412
FDA UDI
Class IActive
Bbig TR21639425
FDA UDI
Class IActive

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