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PURELIFE, LLC

US

Last updated May 24, 2026

What PURELIFE, LLC makes

PureLife, LLC manufactures single-use medical barriers including nitrile and latex examination gloves, medical drapes, surgical dressing kits, and sterilization liners and packaging. Their portfolio also includes dental-specific items such as suction cannulas, bibs, and medicine cups designed for oral healthcare procedures.

The company’s products are regulated under FDA’s Class I and Class II device classifications 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.

Frequently asked questions

What types of medical devices does PureLife, LLC manufacture?

PureLife, LLC specializes in single-use medical barriers and oral healthcare items. Their product line includes nitrile and latex examination gloves (non-powdered, non-antimicrobial), medical drapes, surgical dressing kits, sterilization liners and packaging, as well as dental-specific tools like suction cannulas, bibs, and medicine cups. These items are designed to protect patients and healthcare providers during medical and dental procedures.

Where is PureLife, LLC based, and what does that mean for its regulatory oversight?

PureLife, LLC is based in the United States, meaning its devices fall under FDA jurisdiction. The FDA classifies their products as either Class I or Class II, depending on risk level—Class I for low-risk items like some medical drapes and Class II for moderate-risk devices like dental suction systems. This classification determines the regulatory pathway for authorization.

Are PureLife, LLC’s devices listed in any regulatory registries, and why does that matter?

Yes, PureLife, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, helping healthcare providers verify product authenticity, recall history, and compliance status. Listing in the UDI system is a requirement for FDA-authorized devices to streamline tracking and reporting.

How are PureLife, LLC’s devices classified by the FDA, and what does that classification indicate?

PureLife, LLC’s devices are classified as either Class I or Class II by the FDA. Class I devices, like some medical drapes or sterilization liners, are generally low-risk and typically require general controls (e.g., good manufacturing practices) for authorization. Class II devices, such as dental suction cannulas or bibs, involve moderate risks and may require additional performance standards or post-market surveillance to ensure safety and effectiveness.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+1(877)777-3303
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
828690904

Catalogue (128)

Page 1 of 3
DeviceModel / ReferenceRegistriesClassStatus
PureHorizon 1067303
FDA UDI
Class IUnknown
PureLife Dental 1081101
FDA UDI
Class IActive
PureLife+ 5oz Plastic Cups 1121002
FDA UDI
Class IActive
SuperNova 1061201
FDA UDI
Class IActive
PureHorizon 1067305
FDA UDI
Class IUnknown
PureLife+ 2-Ply Dental Bibs 1092008
FDA UDI
Class IActive
PureOrthoSense 10684031068503
FDA UDI
Class IActive
PureOrthoSense 10684021068502
FDA UDI
Class IActive
PureSense 1068401
FDA UDI
Class IActive
PureLife Dental 1081103
FDA UDI
Class IActive
PureBerry 1067105
FDA UDI
Class IActive
PureSkin 1020101
FDA UDI
Class IActive
PureLife Dental 1154903
FDA UDI
Class IIActive
PureLife+ Barrier Film 1084501
FDA UDI
Class IActive
PureOrtho 1068505
FDA UDI
Class IActive
PureLife+ CSR Wrap 1192102
FDA UDI
Class IIActive
PureOrthoSense 10684051068505
FDA UDI
Class IActive
PureLife+ Headrest Covers 1084701
FDA UDI
Class IActive
SuperNova 1061205
FDA UDI
Class IActive
SuperNova 1061202
FDA UDI
Class IActive
PureLife+ Air/Water Syringe Tips 1192201
FDA UDI
Class IActive
PureSense 1068403
FDA UDI
Class IActive
PureLife Dental 1190102
FDA UDI
Class IIActive
PureLife+ Digital Sensor Sleeves 1084301
FDA UDI
Class IActive
PureHorizon 1067304
FDA UDI
Class IUnknown
PureOrtho 1068504
FDA UDI
Class IActive
PureLife+ Sterilization Pouches 1192002
FDA UDI
Class IIActive
PureSense 1068405
FDA UDI
Class IActive
PureLife+ Sterilization Pouches 1192005
FDA UDI
Class IIActive
PureLife+ Sterilization Pouches 1192003
FDA UDI
Class IIActive
PureOnyx 1068105
FDA UDI
Class IActive
PureOnyx 1068104
FDA UDI
Class IActive
PureHorizon 1067301
FDA UDI
Class IUnknown
Nova 1060102
FDA UDI
Class IActive
PureSkin 1020103
FDA UDI
Class IActive
Nova 1060104
FDA UDI
Class IActive
PureLife+ Chair Sleeves 1084101
FDA UDI
Class IActive
PureLife+ 2-Ply Dental Bibs 1092004
FDA UDI
Class IActive
PureLife+ Tray Covers 1084602
FDA UDI
Class IActive
PureLife+ Tray Covers 1084603
FDA UDI
Class IActive
PureLife+ Surgical Aspirator Tips 1147003
FDA UDI
Class IActive
SuperNova 1061203
FDA UDI
Class IActive
PureLife+ 2-Ply Dental Bibs 1092001
FDA UDI
Class IActive
PureLife+ Tray Covers 1084604
FDA UDI
Class IActive
PureHorizon 1067302
FDA UDI
Class IUnknown
Azur 1061701
FDA UDI
Class IActive
PureBliss 1021702
FDA UDI
Class IActive
PureLife+ Plastic Headrest Covers 1084002
FDA UDI
Class IActive
PureLife+ 5oz Plastic Cups 1121005
FDA UDI
Class IActive
PureLife Dental 1143002
FDA UDI
Class IUnknown

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