Skip to content

Coronet SLS-20-925

by CorneaGen

Coronet SLS-20-925 is a Class I device made by CorneaGen, listed in FDA GUDID since 14 Jun 2024 (UDI-DI 00855934007263), 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 Number00855934007263 UDI-DI Date14 Jun 2024ListedStatusListed 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  • Withdrawn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
Coronet
Generic name
Corneal punch set
Model / reference
SLS-20-925
Primary DI / UDI-DI
00855934007263
FDA product code
HRH
GMDN term
Corneal punch set
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Corneal punch set

Similar devices in this category

Other devices filed under Corneal punch set.

Other devices from CorneaGen

See all devices from CorneaGen →

Properties

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