Bbig TL42067206

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number08719616031323 UDI-DI	Date15 Oct 2017Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Bbig
Generic name: Spectacle frame
Model / reference: TL42067206

Primary DI / UDI-DI: 08719616031323
FDA product code: HQZ
GMDN term: Spectacle frame

Device class: Class I
Regulation number: 886.5842
GUDID distribution status: In Commercial Distribution

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Properties

Single use
Premarket exempt

Other properties (13)

Supplied sterile: No
Sterilise before use: No
Implantable: No
Contains latex: No
Prescription use: No
Over-the-counter: No
Convenience kit: No
Combination product: No
HCT/P: No
Lot / batch number: No
Serial number: No
Expiration date: No
Manufacturing date: No