Skip to content

Curad CUR13620

by Medline Industries, Inc.

Curad CUR13620 is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 8 Jun 2023 (UDI-DI 30888277176755), 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 Number30888277176755 UDI-DI Date8 Jun 2023ListedStatusListed 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  • Withdrawn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
Curad
Generic name
Eye patch, single-use
Model / Ref / Catalog
CUR13620
Primary DI / UDI-DI
30888277176755
FDA product code
KGX
GMDN term
Eye patch, single-use
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Eye patch

Similar devices in this category

Other devices filed under Eye patch.

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)