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Kitpack 2-469

by Network Medical Products, Ltd.

Kitpack 2-469 is a Class II device made by Network Medical Products, Ltd., cleared under FDA 510(k) K130117 on 29 Oct 2013 and listed in FDA GUDID since 22 Mar 2022 (UDI-DI 05056100712614), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K130117

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05056100712614 UDI-DI Date22 Mar 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK130117 Date29 Oct 2013DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K130117 decided 29 Oct 2013 Active
  • FDA GUDID UDI-DI 05056100712614 listed 22 Mar 2022 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K130117
  2. Listed FDA GUDID 05056100712614

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Kitpack
Generic name
Ophthalmic sponge
Model / reference
2-469
Primary DI / UDI-DI
05056100712614
510(k) Number
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

Cleared under the same submission (K130117)

and 8 more cleared under K130117

Other devices from Network Medical Products, Ltd.

See all devices from Network Medical Products, Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)