510(k) Report

FDA applicant

Innovative Ophthalmic Products, Inc. (Iop)

Costa Mesa, CA1 decision2015–20150 recalls

FDA records 1 decision for Innovative Ophthalmic Products, Inc. (Iop) (Costa Mesa, CA) in 2015: 1 510(k) clearance. All are in product code KYF (Implant, Eye Valve). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Innovative Ophthalmic Products, Inc. (Iop)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015: 1
2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Innovative Ophthalmic Products, Inc. (Iop) by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KYFImplant, Eye Valve1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K152996Molteno3 Glaucoma ImplantInnovative Ophthalmic Products, Inc. (Iop) · 2015

The one decision as Innovative Ophthalmic Products, Inc. (Iop) →