Quantumtx Pte., Ltd.
SingaporeFDA 510(k) applicant, unverified FDA
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Quantumtx Pte., Ltd. makes
Quantumtx Pte. Ltd. manufactures muscle performance enhancement devices using electromagnetic stimulation technology. Their portfolio includes the Quantum Mitohormesis (QMT) and its variant, the QMT (M2101), designed to stimulate muscle function through targeted electrical impulses.
These devices are classified as Class II under regulatory frameworks, with authorisations listed in the FDA’s 510(k) and UDI registries. The company is based in the United States.
Catalogue
- GUDID
Quantum Mitohormesis (QMT) (M2101) Ref K240348
510(k) 510(k)
Company details
- DUNS number
- 659470592
FDA establishments
- Quantumtx Pte. Ltd. Singapore Central Singapore · SG FEI 3038138457
Frequently asked questions
How many devices does Quantumtx Pte., Ltd. have in the registry?
The registry currently lists 2 devices for Quantumtx Pte., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Quantumtx Pte., Ltd.'s devices?
Among its 2 most recently registered devices, Quantumtx Pte., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Quantumtx Pte., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Quantumtx Pte., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Quantumtx Pte., Ltd. in the registry?
The most recently registered devices listed for Quantumtx Pte., Ltd. include Quantum Mitohormesis (QMT) M2101 and Quantum Mitohormesis (QMT) (M2101).
Which FDA establishments are linked to Quantumtx Pte., Ltd.?
1 FDA establishment is linked to Quantumtx Pte., Ltd. in the registry; they are listed on the company page.