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Shamrock Marketing Co.

US

Last updated May 23, 2026

What Shamrock Marketing Co. makes

The company manufactures single-use examination and treatment gloves made from nitrile, hevea latex, and vinyl, all in non-powdered and non-antimicrobial formulations. These gloves are designed for medical, dental, and clinical procedures where barrier protection is required.

The portfolio consists of Class I medical devices, authorised through FDA 510(k) and UDI registrations. The company’s products are listed in the FDA’s regulatory databases, and 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 Shamrock Marketing Co. manufacture?

Shamrock Marketing Co. specialises in single-use examination and treatment gloves. Their portfolio includes nitrile, hevea-latex, and vinyl gloves, all formulated as non-powdered and non-antimicrobial. These gloves are designed for medical, dental, and clinical settings where barrier protection is essential during procedures.

Where is Shamrock Marketing Co. based?

Shamrock Marketing Co. is headquartered in the United States. The company’s manufacturing focus aligns with FDA regulatory requirements, ensuring compliance for its medical device products.

Which regulatory registries list Shamrock Marketing Co.’s devices?

Shamrock Marketing Co.’s devices are listed in the FDA’s 510(k) premarket notification database and the FDA’s Unique Device Identifier (UDI) system. These registries confirm the devices’ authorised status under Class I classification.

How are Shamrock Marketing Co.’s gloves classified by regulatory authorities?

Shamrock Marketing Co.’s gloves fall under Class I medical device classification, which is the lowest risk category for devices that pose minimal potential harm. This classification is determined by their intended use as single-use barrier protection, requiring only basic regulatory controls like 510(k) clearance and UDI registration.

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

Information

Country
US
Address
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Website
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Email
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Catalogue (32)

DeviceModel / ReferenceRegistriesClassStatus
Action 36013
FDA UDI
Class IActive
Shamrock 10111
FDA UDI
Class IActive
Action 36012
FDA UDI
Class IActive
Shamrock 20212
FDA UDI
Class IActive
Action 17704
FDA UDI
Class IActive
Shamrock 30351/100
FDA UDI
Class IActive
Polysilk 18014
FDA UDI
Class IActive
Polysilk 18011
FDA UDI
Class IActive
Shamrock 20211
FDA UDI
Class IActive
Shamrock 10113
FDA UDI
Class IActive
Shamrock 30311
FDA UDI
Class IActive
Shamrock 30314
FDA UDI
Class IActive
Shamrock 10114
FDA UDI
Class IActive
Shamrock 20213
FDA UDI
Class IActive
Polysilk 18013
FDA UDI
Class IActive
Shamrock 30312
FDA UDI
Class IActive
Shamrock 30313
FDA UDI
Class IActive
Shamrock 30355/100
FDA UDI
Class IActive
Shamrock 30353/100
FDA UDI
Class IActive
Action 36011
FDA UDI
Class IActive
Shamrock 20214
FDA UDI
Class IActive
Shamrock 30352/100
FDA UDI
Class IActive
Action 17702
FDA UDI
Class IActive
Action 36014
FDA UDI
Class IActive
Shamrock 10110
FDA UDI
Class IActive
Shamrock 30350/100
FDA UDI
Class IActive
Shamrock 10112
FDA UDI
Class IActive
Action 17701
FDA UDI
Class IActive
Polysilk 18012
FDA UDI
Class IActive
Shamrock 30354/100
FDA UDI
Class IActive
Action 17703
FDA UDI
Class IActive
Patient Examination Gloves K904697
FDA 510(k)
Class IActive

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