Skip to content

Clear Choice SMI9211B

by Southmedic Incorporated

Clear Choice SMI9211B is a Class I device made by Southmedic Incorporated, listed in FDA GUDID since 2 Oct 2020 (UDI-DI 10620974002854), 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 Number10620974002854 UDI-DI Date2 Oct 2020ListedStatusListed 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  • Withdrawn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
Clear Choice
Generic name
Face splash shield, single-use
Model / Ref / Catalog
SMI9211B
Primary DI / UDI-DI
10620974002854
FDA product code
HOY
GMDN term
Face splash shield, single-use
Device class
Class I
Regulation number
886.4750
GUDID distribution status
In Commercial Distribution

Related devices

Category: Face splash shield, single-use

Similar devices

Other devices filed under FDA product code HOY (Shield, eye, ophthalmic (including sunlamp protective eyewear and post-mydriatic eyewear)).

Other devices from Southmedic Incorporated

See all devices from Southmedic Incorporated →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)