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Fresh Test, LLC

Last updated May 25, 2026

What Fresh Test, LLC makes

Fresh Test, LLC manufactures point-of-care glucose monitoring systems designed for in vitro diagnostic use, providing rapid blood glucose measurements in clinical or home settings.

The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (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.

Information

Country: US
Address: —
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 051998960

Catalogue (15)

Device	Model / Reference	Registries	Class	Status
Fresh Test	50g Powder	FDA UDI	Class II	Unknown
Fresh Test	50g Powder	FDA UDI	Class II	Active
Fresh Test	75g Powder	FDA UDI	Class II	Unknown
Fresh Test	100g Powder	FDA UDI	Class II	Active
Fresh Test	Beverage 100 Gram	FDA UDI	Class II	Active
Fresh Test	Strawberry Basil Lemonade 75g Powder	FDA UDI	Class II	Active
Fresh Test	Beverage 50 Gram	FDA UDI	Class II	Active
Fresh Test	75g Powder	FDA UDI	Class II	Active
Fresh Test	Plain Dextrose 100g Powder	FDA UDI	Class II	Active
Fresh Test	100g Powder	FDA UDI	Class II	Unknown
Fresh Test	Plain Dextrose 50g Powder	FDA UDI	Class II	Active
Fresh Test	Plain Dextrose 75g Powder	FDA UDI	Class II	Active
Fresh Test	Beverage 75 Gram	FDA UDI	Class II	Active
Fresh Test	Strawberry Basil Lemonade 100g Powder	FDA UDI	Class II	Active
Fresh Test	Strawberry Basil Lemondate 50g Powder	FDA UDI	Class II	Active

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