Viscoelastic Injector

by Sight Sciences, Inc. 2 variants

510(k) K143205

Viscoelastic Injector is a Class II device made by Sight Sciences, Inc., cleared under FDA 510(k) K143205 on 5 Dec 2014, active as of 10 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 10 Oct 2026

Documents

510(k) K143205↗

FDA record

Trust

Source FDA 510(k), synced 10 Oct 2026.

Regulatory status

as of registry sync 10 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Special	NumberK143205	Date5 Dec 2014Cleared	StatusActive

Official records

FDA 510(k) database 510(k) number K143205

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K143205
FDA product code: MRH

Device class: Class II
Regulation: 21 CFR Part 880.5725
Advisory committee: General Hospital
FDA decision: SESE Substantially Equivalent

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