FDA applicant

Ocular Blood Flow Laboratories, Inc.

Timonium, MD2 decisions1987–19870 recalls

FDA records 2 decisions for Ocular Blood Flow Laboratories, Inc. (Timonium, MD) in 1987: 2 510(k) clearances. All are in product code HKX (Tonometer, Ac-Powered). 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 Ocular Blood Flow Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ocular Blood Flow Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ocular Blood Flow Laboratories, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Ocular Blood Flow Laboratories, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Ocular”

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

Ocular Instruments, Inc. 50 Ocular Sciences Puerto Rico, Inc. 7 Ocular Therapeutix, Inc. 2 Ocular Sciences 2 Ocular Innovations, Inc. 2 Ocular Concepts, LLC 1 Ocular Pharmaceuticals, Inc. 1 Ocular Systems, Inc. 1

Ocular Blood Flow Laboratories, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Ocular”