Skip to content

S4 Optik DR 2200

by Lombart Brothers, Inc.

S4 Optik DR 2200 is a Class I device made by Lombart Brothers, Inc., listed in FDA GUDID since 18 Oct 2025 (UDI-DI 00860014277542), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860014277542 UDI-DI Date18 Oct 2025ListedStatusListed 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  • Withdrawn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
S4 Optik
Generic name
Phoropter, electric
Model / reference
DR 2200
Primary DI / UDI-DI
00860014277542
FDA product code
HKN
GMDN term
Phoropter, electric
Device class
Class I
Regulation number
886.1770
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HKN (Refractor, Manual, Non-Powered, Including Phoropter).

Other devices from Lombart Brothers, Inc.

See all devices from Lombart Brothers, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)