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Eyetec 1-411

by Network Medical Products, Ltd.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05056100707115 UDI-DI Date25 Feb 2020ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Eyetec
Generic Name
Ophthalmic sponge
Model / Reference
1-411
Primary DI / UDI-DI
05056100707115
510(k) Number
FDA Product Code
HOZ
GMDN Term
Ophthalmic sponge
Device Class
Class II
Regulation Number
886.4790
GUDID distribution status
Not in Commercial Distribution

Related devices

Cleared under the same submission (K130117)

Show all (12)

Other devices from Network Medical Products, Ltd.

See all devices from Network Medical Products, Ltd. →

Properties

  • Sterile
  • Single Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No