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DOLGENCORP, LLC

US

Last updated May 30, 2026

What DOLGENCORP, LLC makes

DolgenCorp, LLC manufactures menstrual hygiene products including unscented and scented tampons and pads, as well as oral health devices such as manual and electric toothbrushes and dental floss. They also produce a rapid in-vitro diagnostic (IVD) kit for detecting human chorionic gonadotropin (hCG) in clinical settings.

The company’s products are classified under FDA’s Class I and Class II categories, with some listed as unclassified (U), and are registered in the FDA’s Unique Device Identifier (UDI) database. DolgenCorp, LLC 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 DolgenCorp, LLC manufacture?

DolgenCorp, LLC produces a variety of medical devices primarily focused on personal hygiene and oral care. Their portfolio includes menstrual hygiene products like unscented and scented tampons and pads, as well as oral health devices such as manual and electric toothbrushes and dental floss. Additionally, they manufacture a rapid in-vitro diagnostic (IVD) kit designed for detecting human chorionic gonadotropin (hCG) in clinical settings, which is used to confirm pregnancy.

Where is DolgenCorp, LLC based?

DolgenCorp, LLC is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.

Which regulatory registries list DolgenCorp, LLC’s devices?

DolgenCorp, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices by assigning a unique identifier to each product, which helps in tracking and monitoring devices throughout their lifecycle.

How are DolgenCorp, LLC’s devices classified by the FDA?

DolgenCorp, LLC’s devices fall under different FDA classification categories depending on their risk level and intended use. Most of their products are classified as Class I, which includes low-risk devices like basic hygiene items. Some devices, such as certain menstrual products or diagnostic kits, may be classified as Class II, requiring additional controls due to moderate risk. A few devices are listed as unclassified (U), meaning they do not fall into the standard Class I, II, or III categories but still meet regulatory requirements.

Why do some of DolgenCorp, LLC’s devices appear unclassified (U) in the FDA registry?

The unclassified (U) designation in the FDA registry indicates that these devices do not fit neatly into the standard Class I, II, or III risk-based categories. This could be due to unique features, minimal risk, or regulatory pathways that do not require full classification under traditional FDA guidelines. For example, some basic hygiene products may be deemed low-risk enough to operate under general controls without needing specific classification, though they still undergo regulatory oversight to ensure safety and effectiveness.

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

Information

Country
US
Address
—
Website
xx.xx
LinkedIn
—
Facebook
—
Phone
800-899-7353
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
068331990

Catalogue (110)

Page 2 of 3
DeviceModel / ReferenceRegistriesClassStatus
Rexall 00717201
FDA UDI
Class IActive
DG Health Tampons DG12006U0/4
FDA UDI
Class IIActive
Rexall 31028001
FDA UDI
Class IActive
DG Health Tampons 10005202
FDA UDI
Class IIActive
Rexall 25456001
FDA UDI
Class IActive
Rexall 25449901
FDA UDI
Class IActive
Breeze 34201301
FDA UDI
Class IActive
Rexall 25454301
FDA UDI
Class IActive
Rexall 25456901
FDA UDI
Class IActive
Breeze 33991601
FDA UDI
Class IActive
DG Health Tampons DG12006F/3
FDA UDI
Class IIActive
DG Health Tampons BDGPP18
FDA UDI
Class IIActive
Rexall 25446001
FDA UDI
Class IActive
Rexall 25458201
FDA UDI
Class IActive
Rexall 77-352
FDA UDI
Class IIActive
Rexall Sterile Saline Wound Wash 88-50740-200-00
FDA UDI
UActive
Rexall TPE
FDA UDI
Class IActive
Breeze 34201601
FDA UDI
Class IActive
DG Health Tampons BDGPS18
FDA UDI
Class IIActive
DG Health BDGGP36
FDA UDI
Class IIActive
Breeze 31216401
FDA UDI
Class IActive
DG Health 16944901
FDA UDI
Class IIActive
DGHealth 017276234831
FDA UDI
Class IUnknown
Dollar General One Step Pregnancy Test
FDA UDI
Class IIActive
DG Health Tampons 10003688
FDA UDI
Class IIActive
DG Health Tampons DG12006S0/4
FDA UDI
Class IIActive
DG Health BDGFR18
FDA UDI
Class IIActive
DG Health BDGFC34
FDA UDI
Class IIActive
Rexall One Step Pregnancy Test FPPL
FDA UDI
Class IIUnknown
DG Health Tampons DGD91601UA
FDA UDI
Class IIActive
DG Health Tampons BDGPP18+3
FDA UDI
Class IIActive
Breeze 33990801
FDA UDI
Class IActive
Rexall UVW
FDA UDI
Class IActive
DG Health Tampons BDGPR18
FDA UDI
Class IIActive
Rexall 25454901
FDA UDI
Class IActive
DG Health Tampons 10002261
FDA UDI
Class IIActive
Breeze 33991501
FDA UDI
Class IActive
Breeze 35672701
FDA UDI
Class IActive
Rexall One Step Pregnancy Test
FDA UDI
Class IIActive
DG Health Tampons 10005133
FDA UDI
Class IIActive
Rexall 77-359
FDA UDI
Class IIActive
DG health One Step Pregnancy Test
FDA UDI
Class IIActive
Breeze 33991101
FDA UDI
Class IActive
Breeze 34201401
FDA UDI
Class IActive
DG Health BDGGC(R/S/P)36
FDA UDI
Class IIActive
Breeze 33990701
FDA UDI
Class IActive
DG Health Tampons DG31806U0/4
FDA UDI
Class IIActive
DG Health Tampons 10005132
FDA UDI
Class IIActive
Rexall One Step Pregnancy Test
FDA UDI
Class IIActive
Breeze 33991301
FDA UDI
Class IActive

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