Interstate All Battery Center

Interstate All Battery Center specializes in portable and mobile rechargeable battery packs, as well as primary batteries designed for single-use applications. These devices are branded under *Interstate All Battery* and are intended for general-purpose use across portable electronics and equipment. The company does not manufacture medical devices in the traditional sense, but its products may be used in medical settings for powering certain portable equipment.

Interstate All Battery Center is based in the United States. Its devices are classified as Class I under U.S. regulatory standards, which typically indicates a low-risk category requiring minimal regulatory oversight. This classification is based on the general-purpose nature of the products, which are not intended to support or sustain human life or be implanted.

Yes, Interstate All Battery Center’s devices are listed in the FDA’s Unique Device Identifier (UDI) Program. This registry ensures traceability and transparency for devices marketed in the U.S., though listing does not imply regulatory approval—it simply confirms compliance with identification requirements for post-market surveillance and reporting.

The company’s products fall under Class I classification in the U.S., which applies to devices posing minimal risk to patients and users. This classification is determined by factors like the device’s intended use, risk potential, and whether it supports life-sustaining functions or is invasive. Since these batteries are general-purpose and not life-critical, they qualify for this lower-risk category.