FDA applicant

Intelligent Sensory Concept SA

Senarclens, CH1 decision2017–20170 recalls

FDA records 1 decision for Intelligent Sensory Concept SA (Senarclens, CH) in 2017: 1 510(k) clearance. All are in product code GEX (Powered Laser Surgical Instrument). Its devices cite 3 predicates, 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, general and plastic surgery panel, where it files most

How often FDA has decided Intelligent Sensory Concept SA’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Intelligent Sensory Concept SA by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Intelligent”

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

Intelligent Hearing Systems 13 Intelligent Implant Systems, LLC 6 Intelligent Medical Devices, Inc. 4 Intelligent Medicine, Inc. 4 Intelligent Orthopaedics, Ltd. 3 Intelligent Medical Systems 2 Intelligent Ultrasound Limited 2 Intelligent Surgical Lasers, Inc. 2 Intelligent Product Limited Co. 2 Intelligent Images Srl 2 Intelligent Software Systems, Inc. 1 Intelligent Medica Imaging, Inc. 1

Intelligent Sensory Concept SA

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Intelligent”