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Sign in to claim this brandMedical Technology Mix, Inc.
US
Last updated May 23, 2026
What Medical Technology Mix, Inc. makes
Medical Technology Mix, Inc. manufactures an M T M circuit classified as a Class I medical device.
The device is regulated under the FDA 510(k) pathway and the company 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 type of medical device does Medical Technology Mix, Inc. manufacture?
Medical Technology Mix, Inc. produces a single product identified as an M T M circuit. This conclusion is drawn directly from the device list, which only mentions that specific circuit, indicating it is the company's manufacturing focus.
Where is Medical Technology Mix, Inc. headquartered?
The company is based in the United States, as indicated by the COUNTRY field in the provided data. No other location is mentioned, so the U.S. is the sole listed country of operation.
Which regulatory registry lists the M T M circuit and how is it classified?
The M T M circuit is listed in the FDA 510(k) registry, which is the pathway for devices that require premarket notification. The device is classified as Class I, meaning it is considered low risk according to the FDA classification system, as stated in the DEVICE CLASSES and LISTED IN sections.
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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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
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Catalogue (37)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Texas Medical Technology | GWS-03-XL-B | FDA UDI | Class II | Active |
| Texas Medical Technology | GWL-04-SMS-S | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| HeadaTerm | YF-HT2 | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| Texas Medical Technology | GWS-03-5XL-B | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| Texas Medical Technology | GWS-03-XXL-B | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| Texas Medical Technology | 3PLY-PRCMSK-04 | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| Texas Medical Technology | GWS-03-S-B | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E2 | FDA UDI | Class II | Active |
| HeadaTerm | YF-HT-W1 | FDA UDI | Class II | Active |
| Texas Medical Technology | GWL-04-SMS-M | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| Texas Medical Technology | GWL-04-SMS-XL | FDA UDI | Class II | Active |
| Texas Medical Technology | GWL-04-SMS-L | FDA UDI | Class II | Active |
| Texas Medical Technology | GWS-03-3XL-B | FDA UDI | Class II | Active |
| Texas Medical Technology | GWS-03-M-B | FDA UDI | Class II | Active |
| EmeTerm 2 | YF-ZTY-E2 | FDA UDI | Class II | Active |
| Texas Medical Technology | GWS-03-4XL-B | FDA UDI | Class II | Active |
| Texas Medical Technology | GWS-03-L-B | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| HeadaTerm | YF-HT-W1 | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| EmeTerm | YF-ZTY-E1 | FDA UDI | Class II | Active |
| Texas Medical Technology | GWL-04-SMS-2XL | FDA UDI | Class II | Active |
| TENS device-EmeTerm 2, Model: YF-ZTY-E2 | K220503 | FDA 510(k) | Class II | Active |
| Modulap | K982445 | FDA 510(k) | Class II | Active |
| Laser Backpointer Assembly, Mod. 01-2487 | K800489 | FDA 510(k) | Class I | Active |
| TENS device-HeadaTerm 2 (Model: YF-HT2) | K230782 | FDA 510(k) | Class II | Active |
| M T M Circuit | K821086 | FDA 510(k) | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Sep 1, 2022 | Z-0242-2023 | — | open, classified | Surgical gowns recalled due to gown fabric failing to pass the hydrostatic pressure test so the fabric does not provide the protection needed in a level 3 surgical gown, i.e., blood and other fluid may penetrate the fabric. |
FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Wat Medical Technology Inc. Ningbo Zhejiang · CN FEI 3014649088