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Sign in to claim this brandKaVo Dental GmbH
Germany·DE-MF-000006471
Last updated September 17, 2026
What KaVo Dental GmbH makes
KaVo Dental GmbH manufactures ultrasonic dental scaling and debridement systems, dental power tool handpieces (both line-powered and pneumatic), dental delivery systems, dental surgical power tool motors (electric), dental caries detectors using optical induced fluorescence, dental abrasive air jet system handpieces, and dentifrice products. Specific examples include dental treatment units, dental turbines with MULTIflex connectors, SURGmatic S11 C, PROPHYflex powder cherry, SONICflex prep gold Tip No. 49 (A), SONICflex micro Tip No. 32 (A), and INTRA Kopf L67.
The company's devices are classified as Class I, Class II, and Class IIa under regulatory frameworks and are listed in the Eudamed and FDA UDI registries. KaVo Dental GmbH is based in Germany (DE).
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of devices does KaVo Dental GmbH manufacture?
KaVo Dental GmbH manufactures ultrasonic dental scaling and debridement systems, dental power tool handpieces (both line-powered and pneumatic), dental delivery systems, dental surgical power tool motors (electric), dental caries detectors using optical induced fluorescence, dental abrasive air jet system handpieces, and dentifrice products. This is based solely on the device categories and examples provided in the source data, which list these as the core product types without specifying quantities or market reach.
Where is KaVo Dental GmbH based?
KaVo Dental GmbH is based in Germany, as indicated by the country code DE in the device data. This location is explicitly stated in the SUMMARY section and confirmed by the COUNTRY field, with no additional details about facilities, headquarters, or operational sites provided or inferred.
In which regulatory registries are KaVo Dental GmbH's devices listed?
KaVo Dental GmbH's devices are listed in the Eudamed and FDA UDI registries, as directly stated in the LISTED IN field and reiterated in the SUMMARY. These are the only two registries mentioned in the source data, and no others are referenced or implied.
How are KaVo Dental GmbH's devices classified under regulatory frameworks?
KaVo Dental GmbH's devices are classified as Class I, Class II, and Class IIa, as explicitly stated in the DEVICE CLASSES field and repeated in the SUMMARY. This classification reflects the risk-based categorization applied to individual devices, not the company itself, and no further breakdown by device type is provided in the source.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Germany
- Address
- 39, Bismarckring, Biberach, Germany
- Website
- www.kavo.com
- —
- —
- [email protected]
- Phone
- +49 7351 56-0
- PRRC Contact
- Klaus Michael Reisenauer
- EUDAMED SRN
- DE-MF-000006471
- FDA FEI Number
- 3003637274
- DUNS Number
- 333710619
Catalogue (366)
Page 3 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ELECTROmatic T2M-S | 1.013.0311 | FDA UDI | Class I | Active |
| SONICflex prep gold Tip No. 50 (A) | 1.006.1984 | FDA UDI | Class II | Active |
| SMARTtorque LUX S619 L | 1.008.1641 | FDA UDI | Class I | Active |
| SMARTmatic S10 K | 1.011.6731 | FDA UDI | Class I | Active |
| INTRAflex LUX2 2325 LN | 0.535.6210 | FDA UDI | Class I | Active |
| SONICflex scaler Tip No. 5 | 0.571.5171 | FDA UDI | Class II | Active |
| INTRA Kopf L68 B | 1.008.1834 | FDA UDI | Class I | Active |
| SONICflex cem Tip No. 12 | 0.571.5431 | FDA UDI | Class II | Active |
| SONICflex prep crown plain no. 98 A | 1.008.6386 | FDA UDI | Class II | Active |
| EXPERTmatic E20 L | 1.007.5540 | FDA UDI | Class I | Active |
| EXPERT LUX Case 680465LRN | 1.009.6048 | FDA UDI | Class I | Active |
| INTRA Surgery Handpiece 3610 N1 | 0.524.5600 | FDA UDI | Class I | Active |
| INTRA reducing Head 67RIC | 0.540.8340 | FDA UDI | Class I | Active |
| ELECTROtorque TLC 4893 (Set) | 1.003.5840 | FDA UDI | Class I | Active |
| ELECTROmatic TM | 1.011.2100 | FDA UDI | Class I | Active |
| SMARTmatic PROPHY S19 K | 1.011.6741 | FDA UDI | Class I | Active |
| SONICflex cari-ex TC Tipset (A) | 1.006.2032 | FDA UDI | Class II | Active |
| SONICflex scaler Tip No. 7 (A) | 1.005.8951 | FDA UDI | Class II | Active |
| SURGmatic Head S201 L Pro | 1.013.8648 | FDA UDI | Class I | Active |
| Prophylaxe Set 2003 | 1.007.2971 | FDA UDI | Class I | Active |
| ELECTROmatic M-S | 1.012.8537 | FDA UDI | Class I | Active |
| SONICflex cari-ex D Tipset | 1.000.7378 | FDA UDI | Class II | Active |
| INTRA Head CL 3 | 1.001.8993 | FDA UDI | Class I | Active |
| SONICflex scaler Tip No. 8 | 0.571.5371 | FDA UDI | Class II | Active |
| SONICflex rootplaner Tip No. 26 (A) | 1.006.1961 | FDA UDI | Class II | Active |
| SONICflex 2008 L (Set) | 1.007.1607 | FDA UDI | Class II | Active |
| INTRAmatic 23 ES | 1.004.5380 | FDA UDI | Class I | Active |
| PiezoLED | 1.007.3995 | FDA UDI | Class II | Active |
| DIAGNOcam Vision Full HD | 1.013.1500 | FDA UDI | Class II | Active |
| ELECTROmatic TMM/TMC | 1.011.2600 | FDA UDI | Class I | Active |
| SONICflex clean Brush No. 5 | 0.571.0472 | FDA UDI | Class II | Active |
| GENTLEpower LUX 25 LPR | 1.007.3580 | FDA UDI | Class I | Active |
| PROPHYflex powder orange | 1.007.0014 | FDA UDI | Class I | Active |
| MULTIflex Coupling 457 | 0.553.1210 | FDA UDI | Class I | Active |
| SMARTmatic S20 | 1.011.6750 | FDA UDI | Class I | Active |
| SMARTmatic S10 S | 1.011.6732 | FDA UDI | Class I | Active |
| SONICflex prep crown plain No. 98 | 1.008.6385 | FDA UDI | Class I | Active |
| SONICflex clean Brush No. 1 | 0.571.0402 | FDA UDI | Class II | Active |
| EXPERTsurg LUX | 1.008.3500 | FDA UDI | Class I | Active |
| SONICflex scaler Tip No. 6 (A) | 1.005.8950 | FDA UDI | Class II | Active |
| SONICflex paro Tip No. 61 | 0.571.7412 | FDA UDI | Class II | Active |
| SONICflex clean Tip No. 48 | 0.571.0401 | FDA UDI | Class II | Active |
| GENTLEpower LUX 7 LP | 1.001.7452 | FDA UDI | Class I | Active |
| SONICflex rootplaner Tip No. 26 | 0.571.5641 | FDA UDI | Class II | Active |
| INTRA Surgery Handpiece 3624 N | 0.534.5660 | FDA UDI | Class I | Active |
| PROPHYflex perio tip | 2.000.0922 | FDA UDI | Class I | Active |
| SONICflex scaler Tip No. 5 (A) | 1.005.8949 | FDA UDI | Class II | Active |
| SONICflex 2008 L | 1.005.9310 | FDA UDI | Class II | Active |
| GENTLEpower LUX 20 LP | 1.001.7453 | FDA UDI | Class I | Active |
| Prophylaxe Set 2008L/2018 violett | 1.007.6550 | FDA UDI | Class I | Active |
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