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DeRoyal 17-052

by Deroyal Industries, Inc.

DeRoyal 17-052 is a Class II device made by Deroyal Industries, Inc., listed in FDA GUDID since 12 Sep 2016 (UDI-DI 00749756030823), 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 Number00749756030823 UDI-DI Date12 Sep 2016ListedStatusListed 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  • Withdrawn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
DeRoyal
Generic name
Ophthalmic sponge
Model / reference
17-052
Primary DI / UDI-DI
00749756030823
FDA product code
HOZ
GMDN term
Ophthalmic sponge
Device class
Class II
Regulation number
886.4790
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic sponge

Similar devices in this category

Other devices filed under Ophthalmic sponge.

Other devices from Deroyal Industries, Inc.

See all devices from Deroyal Industries, Inc. →

Properties

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