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STORK IB2C, INC., THE

US Last updated 27 May 2026

Devices
7
Registries
GUDID
FDA recalls
0

Catalogue7

What STORK IB2C, INC., THE makes

The company manufactures single-use cervical caps designed for over-the-counter contraceptive use, intended to be inserted into the cervix to block sperm.

These products fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identification (UDI) database. The manufacturer 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 types of medical devices does Stork IB2C, Inc., The manufacture?

Stork IB2C, Inc., The specializes in single-use cervical caps intended for over-the-counter contraceptive use. These devices are designed to be inserted into the cervix to physically block sperm, providing a barrier method of contraception.

Where is Stork IB2C, Inc., The based?

Stork IB2C, Inc., The is headquartered in the United States. The company’s location is relevant for regulatory compliance and distribution, as it operates within the U.S. healthcare and medical device landscape.

Which regulatory registries list Stork IB2C, Inc., The’s devices?

Stork IB2C, Inc., The’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers and regulators to verify product details and compliance.

How are Stork IB2C, Inc., The’s devices classified by regulatory authorities?

Stork IB2C, Inc., The’s cervical caps fall under FDA Class II classification. This classification indicates moderate regulatory oversight, typically reserved for devices that pose a lower risk but still require validation of safety and performance through specific controls.

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

Information

Country
US
Website
rinovum.com
Phone
412-200-7996
DUNS number
968804521