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Sign in to claim this brandMEDICAL TECHNIQUE, INC.
US
Last updated May 24, 2026
What MEDICAL TECHNIQUE, INC. makes
Medical Technique, Inc. manufactures single-use, sterile drapes and bandages for medical procedures, including instrument/equipment drapes and non-latex pressure bandages. They also produce disposable restraints for limbs, torsos, and heads, as well as arm restraints designed for patient immobilization.
The company’s products are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Medical Technique, 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 types of medical devices does Medical Technique, Inc. manufacture?
Medical Technique, Inc. specializes in single-use, sterile medical devices primarily focused on drapes and restraints. Their most common products include instrument/equipment drapes, non-latex pressure bandages, limb/torso/head restraints, and arm restraints. These items are designed for use in medical procedures to maintain sterility and patient immobilization.
Where is Medical Technique, Inc. based?
Medical Technique, Inc. is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework, as it operates under U.S. medical device regulations.
Which regulatory registries list Medical Technique, Inc.’s devices?
Medical Technique, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their products under the FDA’s classification system, ensuring transparency and traceability for healthcare providers and regulators.
How are Medical Technique, Inc.’s devices classified by the FDA?
Medical Technique, Inc.’s devices fall under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional regulations due to moderate risk. The classification depends on the device’s purpose and potential impact on patient safety.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- mtidrape.com
- —
- —
- [email protected]
- Phone
- 520-733-7999
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 790514756
Catalogue (134)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Optics One | MTI-412 | FDA UDI | Class I | Active |
| Optics One | 1295-20 | FDA UDI | Class II | Active |
| Optics One | 4339-20 | FDA UDI | Class II | Active |
| Optics One | 1012-40 | FDA UDI | Class II | Active |
| Optics One | 5441-UC | FDA UDI | Class II | Active |
| Optics One | 5940-64GL | FDA UDI | Class II | Active |
| Optics One | 2722 | FDA UDI | Class II | Active |
| Optics One | 1289-20 | FDA UDI | Class II | Active |
| Optics One | 9414-40 | FDA UDI | Class II | Active |
| Optics One | MTI-001 | FDA UDI | Class II | Active |
| Optics One | 8905-96 | FDA UDI | Class II | Active |
| Optics One | MTI-409 | FDA UDI | Class I | Active |
| Optics One | 3279-50 | FDA UDI | Class II | Active |
| Optics One | 9974-14 | FDA UDI | Class II | Active |
| Optics One | M840-62 | FDA UDI | Class II | Active |
| Optics One | 1290-20 | FDA UDI | Class II | Active |
| Optics One | BB4040RT | FDA UDI | Class II | Active |
| Optics One | 9926-NS | FDA UDI | Class II | Active |
| Optics One | MTI-309 | FDA UDI | Class I | Active |
| Optics One | 9951-20 | FDA UDI | Class II | Active |
| Optics One | G1295-20 | FDA UDI | Class II | Active |
| Optics One | 4840-120 | FDA UDI | Class II | Active |
| Optics One | 9975-14 | FDA UDI | Class II | Active |
| Optics One | MTI-0020 | FDA UDI | Class II | Active |
| Optics One | 4708-40 | FDA UDI | Class II | Active |
| Optics One | 9956-50 | FDA UDI | Class II | Active |
| Optics One | 5950-150 | FDA UDI | Class II | Active |
| Optics One | 9955-50 | FDA UDI | Class II | Active |
| Optics One | 4840-105GL | FDA UDI | Class II | Active |
| Optics One | 1288-20 | FDA UDI | Class II | Active |
| Optics One | BB3020R | FDA UDI | Class II | Active |
| Optics One | 4336-20 | FDA UDI | Class II | Active |
| Optics One | 5450-UC | FDA UDI | Class II | Active |
| Optics One | VPC0696 | FDA UDI | Class II | Active |
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