Surgitel
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Surgitel is a medical device manufacturer, with 58 devices listed in FDA GUDID (FDA Class I) as of 12 Nov 2026.
- Devices
- 58
Registry facts
- Registries
- FDA GUDID 58
- Device classes
- FDA Class I 58
- Identifiers
- DUNS 078566956
What Surgitel makes
Surgitel manufactures reusable surgical binoculars and operating room lights designed for use in surgical environments. These devices are intended to enhance visibility and precision during procedures, supporting surgeons and surgical teams.
The company’s products are classified as Class I medical devices and are listed in the FDA’s Unique Device Identification (UDI) database. Surgitel operates from the United States.
Catalogue
Search and filter all 58 devicesShowing 1-50 of 58
Company details
- DUNS number
- 078566956
Frequently asked questions
How many devices does Surgitel have in the registry?
The registry currently lists 58 devices for Surgitel. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgitel's devices?
Among its 50 most recently registered devices, Surgitel has devices listed in FDA GUDID (50 devices).
What risk classes do Surgitel's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Surgitel's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Surgitel in the registry?
The most recently registered devices listed for Surgitel include SurgiTel Surgical 2.0 LED Headlight, SurgiTel MICROEVK300 FLM, SurgiTel Micro LED Headlight and SurgiTel EVK1000 FLM.