FDA applicant

Northland Cataract & Eye Care Clinic

Kansas City, MO1 decision1991–19910 recalls

FDA records 1 decision for Northland Cataract & Eye Care Clinic (Kansas City, MO) in 1991: 1 510(k) clearance. All are in product code KYD (Strip, Schirmer). 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 Northland Cataract & Eye Care Clinic’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Northland Cataract & Eye Care Clinic since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Northland Cataract & Eye Care Clinic by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Northland”

FDA records each applicant name separately; these may or may not be the same firm.

Northland Dental Engineering 1

Northland Cataract & Eye Care Clinic

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Northland”