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Flynt/Amtex, Inc.

US

Last updated May 23, 2026

What Flynt/Amtex, Inc. makes

Flynt/Amtex, Inc. manufactures stockinette, patient surgical drapes (single-use), and cast stockinette. These products are used in medical settings for wound care, surgical procedures, and orthopedic support.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries. Flynt/Amtex, Inc. 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 does Flynt/Amtex, Inc. make?

Flynt/Amtex, Inc. manufactures stockinette, patient surgical drapes (single-use), and cast stockinette. These products are used in medical settings for wound care, surgical procedures, and orthopedic support, as stated in the company summary. The examples provided all reference Tex-Care Medical, which appears to be a product line or brand associated with these device categories.

Where is Flynt/Amtex, Inc. based?

Flynt/Amtex, Inc. is based in the United States, as explicitly stated in the SUMMARY section of the device data. The COUNTRY field also confirms this with the value 'US'. No further details about specific locations within the U.S. are provided in the data.

Which registries list Flynt/Amtex, Inc.'s devices?

Flynt/Amtex, Inc.'s devices are listed in the FDA 510(k) and FDA UDI registries, as indicated in the LISTED IN field of the device data. These are U.S. Food and Drug Administration systems used for tracking medical device submissions and unique device identification. The company itself is not approved or cleared—only individual devices may be authorized through these pathways.

How are Flynt/Amtex, Inc.'s devices classified?

Flynt/Amtex, Inc.'s devices are classified as Class I and Class II medical devices, according to the DEVICE CLASSES field in the provided data. This classification reflects the level of regulatory control required, with Class I being low risk and Class II requiring special controls. The classification applies to the device types they manufacture, such as stockinette and surgical drapes, not to the company as a whole.

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

Information

Country
US
Address
—
Website
—
LinkedIn
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Facebook
—
Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
038730060

Catalogue (230)

Page 5 of 5
DeviceModel / ReferenceRegistriesClassStatus
Tex-Care Medical 91322-436
FDA UDI
Class IActive
Tex-Care Medical 91110-454
FDA UDI
Class IActive
Tex-Care Medical 91300-550
FDA UDI
Class IActive
Tex-Care Medical 81121-060
FDA UDI
Class IActive
Tex-Care Medical 91160-848
FDA UDI
Class IIActive
Tex-Care Medical 91110-340
FDA UDI
Class IActive
Tex-Care Medical 81160-848
FDA UDI
Class IIActive
Tex-Care Medical 91100-818
FDA UDI
Class IActive
Tex-Care Medical 91861-604
FDA UDI
Class IActive
Tex-Care Medical 91330-250
FDA UDI
Class IActive
Tex-Care Medical 91333-300
FDA UDI
Class IActive
Tex-Care Medical 91300-250
FDA UDI
Class IActive
Tex-Care Medical 81120-336
FDA UDI
Class IActive
Tex-Care Medical 81100-804
FDA UDI
Class IActive
Tex-Care Medical 81100-603
FDA UDI
Class IActive
Tex-Care Medical 91861-204
FDA UDI
Class IActive
Tex-Care Medical 91323-800
FDA UDI
Class IActive
Tex-Care Medical 91100-605
FDA UDI
Class IActive
Tex-Care Medical 91110-872
FDA UDI
Class IActive
Tex-Care Medical 91100-304
FDA UDI
Class IActive
Tex-Care Medical 91338-000
FDA UDI
Class IActive
Tex-Care Medical 81120-454
FDA UDI
Class IActive
Tex-Care Medical 91100-808
FDA UDI
Class IActive
Tex-Care Medical 81110-648
FDA UDI
Class IActive
Tex-Care Medical 91120-660
FDA UDI
Class IActive
Tex-Care Medical 91120-654
FDA UDI
Class IActive
Tex-Care Medical 91333-000
FDA UDI
Class IActive
Tex-Care Medical 91160-648
FDA UDI
Class IIActive
Tex-Care Medical 81110-672
FDA UDI
Class IActive
Tex-Care Sterile Stockinette K955749
FDA 510(k)
Class IIActive

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