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Innovative Medical Technologies, Inc.

US

Last updated May 26, 2026

What Innovative Medical Technologies, Inc. makes

The company manufactures medical devices for blood collection and intravenous administration, including invasive and noninvasive blood collection sets, venous butterfly needles, and capillary blood collection tools. Their portfolio also includes adapters for syringes and blood collection tubes, as well as capillary blood transfer tubes and pumps for in vitro diagnostics (IVD).

These devices are regulated under the FDA as Class I and Class II medical products, with some authorised through the 510(k) pathway and listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from 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 Innovative Medical Technologies, Inc. primarily manufacture?

Innovative Medical Technologies, Inc. specializes in devices for blood collection and intravenous administration. Their portfolio includes invasive and noninvasive blood collection sets, venous butterfly needles, capillary blood collection tools, and adapters for syringes and blood collection tubes. They also produce capillary blood transfer tubes and pumps used in in vitro diagnostics (IVD), ensuring compatibility with various diagnostic workflows.

Where is Innovative Medical Technologies, Inc. based, and how does this affect its regulatory oversight?

The company is based in the United States, which means its devices fall under the jurisdiction of the U.S. Food and Drug Administration (FDA). Since the FDA regulates medical devices in the U.S., Innovative Medical Technologies, Inc.’s products are classified under FDA categories—primarily Class I and Class II—depending on their risk level and intended use.

Which regulatory registries or databases list Innovative Medical Technologies, Inc.’s devices?

The company’s devices are authorised through the FDA’s 510(k) pathway for certain products and are included in the FDA’s Unique Device Identifier (UDI) database. These registries ensure traceability and compliance tracking for medical devices in the U.S., helping healthcare providers verify product details and regulatory status.

How are Innovative Medical Technologies, Inc.’s devices classified under FDA regulations?

The company’s devices are classified as either Class I or Class II under FDA regulations. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body part it interacts with.

Why might some of Innovative Medical Technologies, Inc.’s devices require FDA’s 510(k) clearance?

The FDA’s 510(k) pathway applies to devices that are not low-risk (Class I) or do not meet the definition of a Class II device with pre-defined controls. If a device is substantially equivalent to a legally marketed predicate device in terms of technology and safety, it may require a 510(k) submission to demonstrate equivalence. This ensures that newer versions of established devices maintain the same level of safety and performance.

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

Information

Country
US
Address
—
Website
innovativemedtech.com
LinkedIn
—
Facebook
—
Email
[email protected]
Phone
8665201820
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
792740578

Catalogue (47)

DeviceModel / ReferenceRegistriesClassStatus
Quick-Draw Edta Adapter 15-974
FDA UDI
Class IActive
Ultraflo 281
FDA UDI
Class IIUnknown
Ultraflo-R 338
FDA UDI
Class IIActive
Ultraflo-S 285
FDA UDI
Class IIActive
Ultraflo-S 652
FDA UDI
Class IIActive
Ultraflo-S 298
FDA UDI
Class IIActive
Innoset 596123
FDA UDI
Class IIActive
Ultraflo-S 298
FDA UDI
Class IIUnknown
Ultraflo-R 364
FDA UDI
Class IIActive
Ultraflo-R 365
FDA UDI
Class IIActive
Ultraflo-S 297
FDA UDI
Class IIActive
Ultraflo-S 292
FDA UDI
Class IIActive
Ultraflo-S 283
FDA UDI
Class IIActive
Ultraflo-R 363
FDA UDI
Class IIActive
Ultraflo-R 687
FDA UDI
Class IIActive
Ultraflo-S 656
FDA UDI
Class IIActive
Ultraflo-S 296
FDA UDI
Class IIUnknown
Ultraflo-R 336
FDA UDI
Class IIActive
Innovac 15-500
FDA UDI
Class IIActive
Ultraflo 285
FDA UDI
Class IIUnknown
Ultraflo-R 326
FDA UDI
Class IIActive
Ultraflo-S 281
FDA UDI
Class IIActive
Ultraflo-R 323
FDA UDI
Class IIActive
Ultraflo-T 810
FDA UDI
Class IActive
Ultraflo-V 608
FDA UDI
Class IIActive
Ultraflo-R 335
FDA UDI
Class IIActive
Ultraflo-S 296
FDA UDI
Class IIActive
Quick-Draw Plain Adapter 15-900
FDA UDI
Class IActive
Ultraglide 283
FDA UDI
Class IIUnknown
Innoset 596125
FDA UDI
Class IIUnknown
Ultraflo-S 653
FDA UDI
Class IIActive
Ultraflo-R 324
FDA UDI
Class IIActive
Ultraflo-A 902
FDA UDI
Class IActive
Ultraflo 283
FDA UDI
Class IIUnknown
Ultraflo-R 689
FDA UDI
Class IIActive
Ultraglide 285
FDA UDI
Class IIUnknown
Innoset 596121
FDA UDI
Class IIUnknown
Ultraflo-V 607
FDA UDI
Class IIActive
Ultraflo-R 688
FDA UDI
Class IIActive
Ultraglide 281
FDA UDI
Class IIUnknown
Quick-Draw Heparin Adapter 15-980
FDA UDI
Class IActive
Quick-Draw Capillary Whole Blood Collection System K972969
FDA 510(k)
Class IActive
UltraFlo-R Push Button Blood Collection Set K220458
FDA 510(k)
Class IIActive
Imt Ultrasonic Stride Monitor K854194
FDA 510(k)
N/AActive
Carpal Box K936087
FDA 510(k)
Class IIActive
Improve Blood Collection Set And Improsafe Blood Collection Set K123987
FDA 510(k)
Class IIActive
Rapid Immobilization Device Or R.i.d. System K904237
FDA 510(k)
Class IActive

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