Eclipse, Inc.
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Eclipse, Inc. is a medical device manufacturer, with 49 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 49
Registry facts
- Registries
- FDA GUDID 48
- FDA 510(k) 1
- Device classes
- FDA Class II 20
What Eclipse, Inc. makes
Eclipse, Inc. manufactures single-use blood collection sets for invasive procedures, as well as haematological concentrate systems designed for processing platelet-rich plasma (PRP). Their portfolio includes hypodermic needles for medical use and professional-grade cosmetic micro-needling devices, including electronic handpieces and disposable micro-cannula cartridges for dermatological treatments.
The company’s devices are classified under FDA Class II regulations and are listed in the FDA’s 510(k) and UDI registries.
Catalogue
Search and filter all 49 devicesFrequently asked questions
How many devices does Eclipse, Inc. have in the registry?
The registry currently lists 49 devices for Eclipse, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eclipse, Inc.'s devices?
Among its 49 most recently registered devices, Eclipse, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (48 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Eclipse, Inc.'s devices fall under?
Among its 49 most recently registered devices, the classes recorded for Eclipse, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eclipse, Inc. in the registry?
The most recently registered devices listed for Eclipse, Inc. include Eclipse PRP HC PRP2700.CAN, Eclipse DermaFlex MicroCannula DF27G50MM26G, Eclipse Cosmetic Applicator Kit CA-100-00-02 and Eclipse Cosmetic Applicator Kit CA-100-00-01.