Bd Visidrape Ophthalmic Drapes; Bd Visiflex Incise Drape

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K010572 ↗

FDA Product Code

KKX

Models / Variants

Bd Visidrape Ophthalmic Drapes

Bd Visiflex Incise Drape

FDA applicant

Becton, Dickinson and Co.

Device Class

Class II

Regulation

21 CFR Part 878.4370

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

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See all devices from Becton, Dickinson & Co. →