Eyetec 1-417

by Network Medical Products, Ltd.

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

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

in data synced 22 Oct 2026

Documents

FDA submission, from GUDID

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number05056100707191 UDI-DI	Date25 Feb 2020Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK130117	Date29 Oct 2013Decided	StatusActive

Official records

AccessGUDID record UDI-DI 05056100707191
FDA 510(k) database 510(k) number K130117

Recalls

0 recalls · FDA

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

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Eyetec
Generic name: Ophthalmic sponge
Model / reference: 1-417

Primary DI / UDI-DI: 05056100707191
510(k) Number: K130117
FDA product code: HOZ
GMDN term: Ophthalmic sponge

Device class: Class II
Regulation number: 886.4790
GUDID distribution status: In Commercial Distribution

Other devices from Network Medical Products, Ltd.

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See all devices from Network Medical Products, Ltd. →

Properties

Supplied sterile
Single use
Lot / batch number
Expiration date

Other properties (11)

Sterilise before use: No
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