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SEQUEL MED TECH, LLC

US

Last updated May 30, 2026

What SEQUEL MED TECH, LLC makes

Sequel Med Tech, LLC makes ambulatory insulin infusion pump/interstitial glucose monitoring systems. The specific device they produce is called the twiist.

The twiist device is classified as Class II and is listed in the FDA UDI registry. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Sequel Med Tech, LLC make?

Sequel Med Tech, LLC makes ambulatory insulin infusion pump/interstitial glucose monitoring systems, specifically the twiist device, as stated in the provided device data.

Where is Sequel Med Tech, LLC based?

Sequel Med Tech, LLC is based in the United States, as indicated in the country field of the device data.

Which registry lists the devices made by Sequel Med Tech, LLC?

The devices made by Sequel Med Tech, LLC are listed in the FDA UDI registry, as specified in the LISTED IN field of the device data.

How are the devices made by Sequel Med Tech, LLC classified?

The devices made by Sequel Med Tech, LLC are classified as Class II, as stated in the DEVICE CLASSES field of the device data.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
877-489-4478
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
119070341

Catalogue (8)

DeviceModel / ReferenceRegistriesClassStatus
twiist DKPI-21073-007
FDA UDI
Class IIActive
twiist RF-90100
FDA UDI
Class IIActive
twiist CM-10100
FDA UDI
Class IIActive
twiist DKPI-11073-001
FDA UDI
Class IIActive
twiist RF-90400
FDA UDI
Class IIActive
twiist DKPI-11099-001
FDA UDI
Class IIActive
twiist DKPI-11029-007
FDA UDI
Class IIActive
twiist DKPI-11098-001
FDA UDI
Class IIActive

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