Mumease
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Mumease is a medical device manufacturer, with 8 devices listed in FDA GUDID and FDA 510(k) (FDA Unclassified) as of 14 Nov 2026.
- Devices
- 8
Registry facts
- Registries
- FDA GUDID 7
- FDA 510(k) 1
- Device classes
- FDA Unclassified 8
What Mumease makes
Mumease manufactures acupressure wristbands designed to provide targeted pressure relief for symptoms associated with menstrual discomfort. The devices are marketed as wearable bracelets intended for temporary relief of cramping and related tension.
The company’s portfolio is classified under FDA Class II devices and is authorised via 510(k) clearances and the FDA’s Unique Device Identifier (UDI) system. These products are listed in the US regulatory framework and comply with applicable medical device regulations.
Catalogue
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
TumEase Acupressure Bracelets Ref K193374
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mumease have in the registry?
The registry currently lists 8 devices for Mumease. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mumease's devices?
Among its 8 most recently registered devices, Mumease has devices listed in FDA 510(k) (1 device) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What are the newest devices from Mumease in the registry?
The most recently registered devices listed for Mumease include TumEase B6, MumEase AB1, TumEase B1 and TumEase B2.