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Penlight S222-BLK

by Rashman Corp.

Penlight S222-BLK is a Class I device made by Rashman Corp., listed in FDA GUDID since 2 Dec 2022 (UDI-DI 00786511390532), 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 Number00786511390532 UDI-DI Date2 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  • Withdrawn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
Penlight
Generic name
Corneal marker handpiece
Model / reference
S222-BLK
Primary DI / UDI-DI
00786511390532
FDA product code
KYT
GMDN term
Corneal marker handpiece
Device class
Class I
Regulation number
880.6350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Corneal marker handpiece

Similar devices

Also classified as Corneal marker handpiece.

Similar devices

Other devices filed under FDA product code KYT (Light, Examination, Medical, Battery Powered).

Other devices from Rashman Corp.

See all devices from Rashman Corp. →

Properties

  • Premarket exempt
Other properties (14, all answered No)