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Sign in to claim this brandXemis Medical Technology (Shenzhen) Co., Ltd.
US
Last updated May 31, 2026
What Xemis Medical Technology (Shenzhen) Co., Ltd. makes
Xemis Medical Technology produces professional-grade cosmetic red-light phototherapy systems, including ultrasound therapy workstations and photon therapy apparatus designed for medical and aesthetic treatments. Their devices are intended for procedures such as skin rejuvenation, tissue repair, and pain management through controlled light and ultrasound therapies.
The company’s portfolio is classified under FDA Class II devices and is listed in the FDA’s 510(k) and UDI registries. 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 Xemis Medical Technology primarily manufacture?
Xemis Medical Technology specializes in professional-grade cosmetic red-light phototherapy systems. Their devices include ultrasound therapy workstations and photon therapy apparatus, which are designed for medical and aesthetic treatments like skin rejuvenation, tissue repair, and pain management. These devices utilize controlled light and ultrasound therapies to deliver targeted therapeutic effects.
Where is Xemis Medical Technology based, and what is its primary focus?
Xemis Medical Technology is based in the United States. The company focuses on developing professional-grade devices for cosmetic and therapeutic applications, particularly in the field of red-light phototherapy and ultrasound-based treatments. Their portfolio is tailored toward medical and aesthetic procedures.
Which regulatory registries list Xemis Medical Technology’s devices?
Xemis Medical Technology’s devices are listed in the FDA’s 510(k) premarket notification registry and the FDA’s Unique Device Identifier (UDI) system. These registries track Class II devices that require regulatory clearance before commercial distribution in the U.S.
How are Xemis Medical Technology’s devices classified under FDA regulations?
Xemis Medical Technology’s devices fall under FDA Class II classification. This classification applies to devices that generally pose moderate risk and require special controls—such as performance standards or post-market surveillance—to ensure safety and effectiveness. Class II devices typically require a 510(k) clearance process.
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
- 847284864
Catalogue (107)
Page 1 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Kumeda | B07 | FDA UDI | Class II | Active |
| Ovutek | F1103T | FDA UDI | Class II | Active |
| Aolstecell | B15 | FDA UDI | Class II | Active |
| Cazon | B26 | FDA UDI | Class II | Active |
| meguo | B15 | FDA UDI | Class II | Active |
| Omk | B02 | FDA UDI | Class II | Active |
| Xemis | BL-10 | FDA UDI | Class II | Active |
| Heallife | B15 | FDA UDI | Class II | Active |
| wellue | B02T | FDA UDI | Class II | Active |
| Nursal | B51 | FDA UDI | Class II | Active |
| Cigii | B56 | FDA UDI | Class II | Active |
| Gpzon | B26 | FDA UDI | Class II | Active |
| Omk | B07 | FDA UDI | Class II | Active |
| lovia | B26 | FDA UDI | Class II | Active |
| Gpzon | B26 | FDA UDI | Class II | Active |
| Alcedo | B21 | FDA UDI | Class II | Active |
| Blood Pressure Monitor | B23 | FDA UDI | Class II | Active |
| cigii | C02 | FDA UDI | Class II | Active |
| Baifros | B15 | FDA UDI | Class II | Active |
| Ciekaa | B21H | FDA UDI | Class II | Active |
| cigii | B15 | FDA UDI | Class II | Active |
| C0mfier | B15 | FDA UDI | Class II | Active |
| Cooceer | B56 | FDA UDI | Class II | Active |
| Homietec | B06T | FDA UDI | Class II | Active |
| ChiSip | B51 | FDA UDI | Class II | Active |
| Blood Pressure Monitor | B22 | FDA UDI | Class II | Active |
| Beegod | B22 | FDA UDI | Class II | Active |
| Fotosy | W1101L | FDA UDI | Class II | Active |
| Mebak | B56 | FDA UDI | Class II | Active |
| metene | B15 | FDA UDI | Class II | Active |
| Hikevan | B01 | FDA UDI | Class II | Active |
| cigii | B15 | FDA UDI | Class II | Active |
| Douhao | C02 | FDA UDI | Class II | Active |
| Oklar | W05 | FDA UDI | Class II | Active |
| Coverich | W05 | FDA UDI | Class II | Active |
| WilBee | C02 | FDA UDI | Class II | Active |
| Fotosy | BA31 | FDA UDI | Class II | Active |
| xingkaiqi | B15 | FDA UDI | Class II | Active |
| Fotosy | W02 | FDA UDI | Class II | Active |
| metene | B13A | FDA UDI | Class II | Active |
| Alofox | B22 | FDA UDI | Class II | Active |
| Zitrads | B22 | FDA UDI | Class II | Active |
| Tenker | B02 | FDA UDI | Class II | Active |
| Beemoon | B26 | FDA UDI | Class II | Active |
| Wellue | B02S | FDA UDI | Class II | Active |
| Medgram | B26 | FDA UDI | Class II | Active |
| Shapa | B06T | FDA UDI | Class II | Active |
| Cigii | B26 | FDA UDI | Class II | Active |
| Panacare | B63 | FDA UDI | Class II | Active |
| Abesee | BN1WC | FDA UDI | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Xemis Medical Technology (shenzhen) Co., Ltd. Shenzhen Guangdong · CN FEI 3038197172