Skip to content

Lulu L181 SLA 53

by Tura Inc.

Lulu L181 SLA 53 is a Class I device made by Tura Inc., listed in FDA GUDID since 1 Dec 2022 (UDI-DI 00764724850319), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00764724850319 UDI-DI Date1 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Lulu
Generic name
Spectacle frame
Model / reference
L181 SLA 53
Primary DI / UDI-DI
00764724850319
FDA product code
HQY
GMDN term
Spectacle frame
Device class
Class I
Regulation number
886.5850
GUDID distribution status
In Commercial Distribution
Size
Width — 53 Millimeter

Related devices

Category: Spectacle frame

Other devices from Tura Inc.

See all devices from Tura Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)