600-15

by Eagle Labs, LLC

600-15 is a Class II device made by Eagle Labs, LLC, listed in FDA GUDID since 28 Oct 2016 (UDI-DI 00810090013510), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00810090013510 UDI-DI	Date28 Oct 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00810090013510

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name: Ophthalmic sponge
Model / reference: 600-15

Primary DI / UDI-DI: 00810090013510
FDA product code: HOZ
GMDN term: Ophthalmic sponge

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

Sterilisation method: Radiation Sterilization

Similar devices in this category

Other devices filed under Ophthalmic sponge.

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Properties

Supplied sterile
Sterilise before use
Single use
Prescription use
Premarket exempt
Lot / batch number
Expiration date
Manufacturing date

Other properties (7, all answered No)