Corneal Transplant Trephine Disposable Blade

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K861825 ↗

FDA Product Code

HRH

Device Class

Class I

Regulation

21 CFR Part 886.4350

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

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See all devices from Storz Instrument Co. →