FDA applicant

Perception, Inc.

Great Neck,, NY4 decisions1997–19980 recalls

FDA records 4 decisions for Perception, Inc. (Great Neck,, NY) from 1997 to 1998: 4 510(k) clearances. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and IYN (System, Imaging, Pulsed Doppler, Ultrasonic). Its devices cite 23 predicates, 3 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, radiology panel, where it files most

How often FDA has decided Perception, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Perception, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Perception, 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 “Perception”

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

Perception Vision Medical Technologies Ltd.Co. 1 Perception Vision Medical Technology Co., Ltd. 1

Perception, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Perception”