Flex 5028-150

by Diversified Products, Inc.

Flex 5028-150 is a Class I device made by Diversified Products, Inc., listed in FDA GUDID since 30 Nov 2022 (UDI-DI 00037741502821), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00037741502821 UDI-DI	Date30 Nov 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00037741502821

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Flex
Generic name: Magnifying spectacles
Model / reference: 5028-150

Primary DI / UDI-DI: 00037741502821
FDA product code: HOI
GMDN term: Magnifying spectacles

Device class: Class I
Regulation number: 886.5840
GUDID distribution status: In Commercial Distribution

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Properties

Over-the-counter
Premarket exempt

Other properties (13, all answered No)