Precision Electrolysis Needles, Inc.
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- Devices
- 1
What Precision Electrolysis Needles, Inc. makes
Precision Electrolysis Needles, Inc. manufactures electrolysis epilation needles designed for hair removal procedures. These devices are intended for use in professional and clinical settings to remove unwanted hair through precise electrolysis techniques.
The company’s portfolio is regulated under FDA’s Class I device classification and requires 510(k) clearance. The devices are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
Epilation Needle Ref K894771
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precision Electrolysis Needles, Inc. have in the registry?
The registry currently lists 1 device for Precision Electrolysis Needles, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precision Electrolysis Needles, Inc.'s devices?
Among its 1 most recently registered device, Precision Electrolysis Needles, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Precision Electrolysis Needles, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Precision Electrolysis Needles, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Precision Electrolysis Needles, Inc. in the registry?
The most recently registered devices listed for Precision Electrolysis Needles, Inc. include EPILATION NEEDLE.