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KMART HOLDING CORPORATION

US

Last updated May 30, 2026

What KMART HOLDING CORPORATION makes

KMART HOLDING CORPORATION manufactures unscented and scented menstrual tampons, basic insulin syringes with needles, and autoinjector needles designed for insulin delivery. Their product line includes disposable tampons and insulin-related devices intended for personal medical use at home.

The company’s devices are classified under Class II by regulatory standards and are listed in the FDA’s Unique Device Identifier (UDI) database. Their portfolio is regulated under US medical device laws, and 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 types of medical devices does KMART HOLDING CORPORATION manufacture?

KMART HOLDING CORPORATION produces menstrual tampons (both unscented and scented), basic insulin syringes with needles, and autoinjector needles specifically designed for insulin delivery. These devices are intended for personal medical use in home settings, covering reproductive health and diabetes management.

Where is KMART HOLDING CORPORATION based?

KMART HOLDING CORPORATION is headquartered in the United States. As a US-based manufacturer, its devices are subject to regulatory oversight under US medical device laws.

Which regulatory registries list KMART HOLDING CORPORATION’s devices?

KMART HOLDING CORPORATION’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance tracking for medical devices authorised under US regulations.

How are KMART HOLDING CORPORATION’s devices classified under regulatory standards?

KMART HOLDING CORPORATION’s devices fall under Class II classification by regulatory standards. This classification applies to products that generally pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
303-271-0300
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
131978533

Catalogue (22)

DeviceModel / ReferenceRegistriesClassStatus
SMART SENSE Tampon BKMPS50
FDA UDI
Class IIActive
Image Essentials One Step Pregnancy Test FPPL
FDA UDI
Class IIUnknown
Smart Sense Insulin Syringes 053108
FDA UDI
Class IIActive
Smart Sense Pen Needles 700001338
FDA UDI
Class IIActive
Guaranteed Quality Products KD-181
FDA UDI
Class IIUnknown
Smart Sense Insulin Syringes 033108
FDA UDI
Class IIActive
SMART SENSE Tampons BKMXC36
FDA UDI
Class IIActive
SMART SENSE Tampons BKMSGP36
FDA UDI
Class IIActive
Image Essentials One Step Pregnancy Test FPPL
FDA UDI
Class IIUnknown
Smart Sense Tampons BKMGR18
FDA UDI
Class IIActive
Smart Sense Tampons BKMSGR18
FDA UDI
Class IIActive
Smart Sense Insulin Syringes 102912
FDA UDI
Class IIActive
SMART SENSE Tampons BKMGR36
FDA UDI
Class IIActive
Smart Sense Tampons BKMGS18
FDA UDI
Class IIActive
Guaranteed Quality Products KD-120
FDA UDI
Class IIUnknown
Smart Sense Tampons BKMSGS18
FDA UDI
Class IIActive
Smart Sense Insulin Syringes 103108
FDA UDI
Class IIActive
Guaranteed Quality Products KD-1631
FDA UDI
Class IIUnknown
Smart Sense Pen Needles 700001337
FDA UDI
Class IIActive
SMART SENSE Tampons BKMUR18
FDA UDI
Class IIActive
Smart Sense Insulin Syringes 052912
FDA UDI
Class IIActive
Smart Sense Early Result Pregnancy Test PLPL
FDA UDI
Class IIUnknown

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