MASUNAGA since 1905 Begonia 19 BK/GP 49

by Masunaga Optical Mfg.co., Ltd.

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	Number04582647303820 UDI-DI	Date15 May 2024Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: MASUNAGA since 1905
Generic Name: Spectacle frame
Model / Reference: Begonia 19 BK/GP 49

Primary DI / UDI-DI: 04582647303820
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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See all devices from Masunaga Optical Mfg.co., Ltd. →

Properties

Premarket Exempt

Other properties (13)

Sterile: No
Single 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