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Watkins-Conti Products, Inc.

US

Last updated May 30, 2026

What Watkins-Conti Products, Inc. makes

Watkins-Conti Products, Inc. manufactures urinary incontinence vaginal inserts, offered in both reusable and single‑use formats. The primary device marketed is the Yoni.Fit Bladder Support, which is designed to provide vaginal support for bladder control.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) database and the FDA UDI system. The company is headquartered 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 Watkins-Conti Products, Inc. make?

Watkins-Conti Products, Inc. manufactures urinary incontinence vaginal inserts, which are available in both reusable and single-use formats. The primary device offered is the Yoni.Fit Bladder Support, designed to provide vaginal support for bladder control. This information is based solely on the provided device data, which specifies these product types and the example device name.

Where is Watkins-Conti Products, Inc. based?

Watkins-Conti Products, Inc. is headquartered in the United States, as explicitly stated in the SUMMARY section of the device data. The COUNTRY field also confirms this location as US. No further details about specific cities, facilities, or operational sites are provided in the data, so the answer is limited to the country level.

Which regulatory registries list Watkins-Conti Products, Inc.'s devices?

The devices manufactured by Watkins-Conti Products, Inc. are listed in the FDA 510(k) database and the FDA UDI (Unique Device Identification) system, as stated in the LISTED IN field and reiterated in the SUMMARY. These are the only registries mentioned in the provided data, and no other domestic or international databases are referenced.

How are Watkins-Conti Products, Inc.'s devices classified?

The devices produced by Watkins-Conti Products, Inc. are classified as Class II medical devices, according to the DEVICE CLASSES field in the provided data. This classification indicates they require special controls to ensure safety and effectiveness, but the data does not state or imply that the company itself is approved, cleared, or certified—only that individual devices fall under this regulatory class.

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

Information

Country
US
Address
—
Website
yonifit.com
LinkedIn
—
Facebook
—
Phone
1-844-966-4348
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
053049687

Catalogue (12)

DeviceModel / ReferenceRegistriesClassStatus
Yoni.Fit Bladder Support PT-1006
FDA UDI
Class IIActive
Yoni.Fit Bladder Support PT-1007
FDA UDI
Class IIActive
Yoni.Fit Bladder Support PT-A-0011
FDA UDI
Class IIActive
Yoni.Fit Bladder Support PT-A-0016
FDA UDI
Class IIActive
Yoni.Fit Bladder Support PT-A-0013
FDA UDI
Class IIActive
Yoni.Fit Bladder Support PT-A-0015
FDA UDI
Class IIActive
Yoni.Fit Bladder Support PT-1004
FDA UDI
Class IIActive
Yoni.Fit Bladder Support PT-A-0012
FDA UDI
Class IIActive
Yoni.Fit Bladder Support PT-1003
FDA UDI
Class IIActive
Yoni.Fit Bladder Support PT-1005
FDA UDI
Class IIActive
Yoni.Fit Bladder Support PT-1002
FDA UDI
Class IIActive
Yoni.Fit Bladder Support K232525
FDA 510(k)
Class IIActive

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