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Sign in to claim this brandLuvo Medical Technologies Inc
Canada·CA-MF-000028601
Last updated May 25, 2026
Information
- Country
- Canada
- Address
- 125, Fleming Drive, Cambridge, Canada
- Website
- www.clarionmedical.com/
- —
- —
- [email protected]
- Phone
- 519-620-3900
- PRRC Contact
- Gregory Berzak
- EUDAMED SRN
- CA-MF-000028601
- FDA FEI Number
- —
- DUNS Number
- 204046564
Catalogue (48)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bela Md+ Aqua Tip | ES2586 | FDA UDI | Class I | Active |
| Bela Md+ Diamond Tip | ES2060 | FDA UDI | Class I | Active |
| Lucent IPL | ESM-9200IL | FDA UDI | Class II | Active |
| Bela Md+ Aqua Tip | ES2587 | FDA UDI | Class I | Active |
| Bela Md+ Aqua Handpiece | 2225-SHP00003 | FDA UDI | Class I | Active |
| Bela MD+ | ESK-2281HD | FDA UDI | Class I | Active |
| Bela Md+ Electroporation Handpiece | 2249-A9900201 | FDA UDI | Class I | Active |
| Darwin IPL Handpiece | 3134 A9999001LV | FDA UDI | Class II | Active |
| Bare: 808 Handpiece | 9300-A0000101 | FDA UDI | Class II | Active |
| Darwin Diode Laser Handpiece | 9300-A0000101LV | FDA UDI | Class II | Active |
| RF Microneedling Handpiece | 3245-A9900201LV | FDA UDI | Class II | Active |
| Darwin RF Thermal | 7600-A99 | FDA UDI | Class II | Active |
| World PRP | WORLDPRP | FDA UDI | Class II | Active |
| Bare 808 | ESM-9300LD | FDA UDI | Class II | Active |
| Darwin | ESK-3272LV | FDA UDI | Class II | Active |
| Bela Md+ Y Handpiece | 2253-A9900201 | FDA UDI | Class I | Active |
| Lucent IPL – handpiece | 3134 A9999001 | FDA UDI | Class II | Active |
| Bela Md+ Skin Scrubber Handpiece | ES0076 | FDA UDI | Class I | Active |
| Lm Anchor | K960448 | FDA 510(k) | Class II | Active |
| Lmt Bone Anchor | K953764 | FDA 510(k) | Class II | Active |
| Lm Bone Anchor (orthopedics) | K963812 | FDA 510(k) | Class II | Active |
| Rotorblade | K983435 | FDA 510(k) | Class II | Active |
| Laporascopic Cannula Seal | K933025 | FDA 510(k) | Class II | Active |
| Lm Anchor | K981755 | FDA 510(k) | Class II | Active |
| Bare: 808 | K193446 | FDA 510(k) | Class II | Active |
| Darwin | K203728 | FDA 510(k) | Class II | Active |
| Ultrasorb Suture Anchor | K002413 | FDA 510(k) | Class II | Active |
| Rotorblade Suture Anchor | K992938 | FDA 510(k) | Class II | Active |
| Lmt Arthroscopic Suturing Instruments | K941964 | FDA 510(k) | Class II | Active |
| Rotorblade Suture Anchor | K993373 | FDA 510(k) | Class II | Active |
| Lucent : IPL | K193072 | FDA 510(k) | Class II | Active |
| Lm Anchor Or Other Proprietary Name | K960825 | FDA 510(k) | Class II | Active |
| Lmt Bone Anchor | K951472 | FDA 510(k) | Class II | Active |
| Lmt Bone Anchor | K951233 | FDA 510(k) | Class II | Active |
| Darwin | K212607 | FDA 510(k) | Class II | Active |
| Lm Bone Anchor | K960439 | FDA 510(k) | Class II | Active |
| RF Thermal System | K210129 | FDA 510(k) | Class II | Active |
| Lm Anchor | K981764 | FDA 510(k) | Class II | Active |
| Lm Bone Anchor | K963288 | FDA 510(k) | Class II | Active |
| Instruments For Laparoscopic Use | K931142 | FDA 510(k) | Class II | Active |
| Powerflex Single Use Fiber (272se-Rt) Delivery Device | 272SE-RT | EUDAMED | Class IIa | Active |
| Powerflex Single Use Fiber (272se-3mm) Delivery Device | 272SE-3MM | EUDAMED | Class IIa | Active |
| Powerflex Single Use Fiber (200se-Rt)delivery Device | 200SE-RT | EUDAMED | Class IIa | Active |
| Powerflex Single Use Fiber (365se-3mm) Delivery Device | 365SE-3MM | EUDAMED | Class IIa | Active |
| Powerflex Single Use (365se-Rt) Fiber Delivery Device | 365SE-RT | EUDAMED | Class IIa | Active |
| Powerflex Single Use Fiber Delivery Device | 550SE | EUDAMED | Class IIa | Active |
| Powerflex Reusable Fiber Delivery Device | 1000R | EUDAMED | Class IIa | Active |
| Powerflex Single Use Fiber Delivery Device | 1000SE | EUDAMED | Class IIa | Active |
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