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Sign in to claim this brandYbeam Technologies, Inc.
US
Last updated May 23, 2026
What Ybeam Technologies, Inc. makes
Ybeam Technologies, Inc. makes the ORLIGHT 2000 Surgical Laser System, a device used for surgical procedures involving laser energy.
The ORLIGHT 2000 Surgical Laser System is classified as a Class II medical device and is listed in the FDA 510(k) registry; 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 does Ybeam Technologies, Inc. make?
Ybeam Technologies, Inc. makes the ORLIGHT 2000 Surgical Laser System, which is a device used for surgical procedures involving laser energy. This is the only example device provided in the data, and no other products are mentioned or implied.
Where is Ybeam Technologies, Inc. based?
Ybeam Technologies, Inc. is based in the United States, as explicitly stated in the country field of the device data. The company’s location is specified as US, which refers to the United States of America.
Which regulatory registries list Ybeam Technologies, Inc.'s devices?
The ORLIGHT 2000 Surgical Laser System made by Ybeam Technologies, Inc. is listed in the FDA 510(k) registry, as indicated in the LISTED IN field. No other registries are mentioned in the provided data.
How are Ybeam Technologies, Inc.'s devices classified?
The ORLIGHT 2000 Surgical Laser System is classified as a Class II medical device, according to the DEVICE CLASSES field. This classification reflects the level of regulatory control required for the device based on its intended use and risk profile.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (283)
Page 6 of 6| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Doselogix | TC140PURPLE | FDA UDI | Class I | Active |
| Doselogix | TC35-CHK | FDA UDI | Class I | Active |
| Doselogix | TC9-A-LIGHTSAFE 3.5ML Micro | FDA UDI | Class I | Active |
| Doselogix | TC9-P-ORANGE | FDA UDI | Class I | Active |
| Doselogix | TC9-R-WHITE | FDA UDI | Class I | Active |
| AllPro | 710 DPA | FDA UDI | Class I | Active |
| Doselogix | TC9-A-LIGHTSAFE-6.5ML ANGLED | FDA UDI | Class I | Active |
| AllPro | Prophy Perfect DPA | FDA UDI | Class I | Active |
| Doselogix | TC9-A-WHITE | FDA UDI | Class I | Active |
| Doselogix | TCPERL01 | FDA UDI | Class I | Active |
| Doselogix | TC35PINK | FDA UDI | Class I | Active |
| Doselogix | TC9-P-GREEN | FDA UDI | Class I | Active |
| AllPro | 102 (Screw) | FDA UDI | Class I | Active |
| Doselogix | TC35SILVER | FDA UDI | Class I | Active |
| Doselogix | TC5-R-LIGHTSAFE | FDA UDI | Class I | Active |
| AllPro | Prophy Perfect DPA | FDA UDI | Class I | Active |
| AllPro | 102 (Screw) | FDA UDI | Class I | Active |
| AllPro | 101 (Screw) | FDA UDI | Class I | Active |
| AllPro | 106 (Screw) | FDA UDI | Class I | Active |
| AllPro | 803 DPA | FDA UDI | Class I | Active |
| AllPro | 211 (Screw) | FDA UDI | Class I | Active |
| AllPro | 103 (Screw) | FDA UDI | Class I | Active |
| AllPro | 302 (Snap On) | FDA UDI | Class I | Active |
| Doselogix | TC9-R-BLUE 3.5ML Micro | FDA UDI | Class I | Active |
| AllPro | 104 (Screw) | FDA UDI | Class I | Active |
| AllPro | Interdental | FDA UDI | Class I | Active |
| Doselogix | TC35 Blue | FDA UDI | Class I | Active |
| AllPro | L106 (Long Screw) | FDA UDI | Class I | Active |
| Disposable Prophylaxis Angle | K941189 | FDA 510(k) | Class I | Active |
| Cytology Brush | K971849 | FDA 510(k) | Class II | Active |
| Bufflight Clt Surgical Laser System | K000727 | FDA 510(k) | Class II | Active |
| Extended Straight Attachment | K994024 | FDA 510(k) | Class I | Active |
| Orlight 2000 Surgical Laser System | K990452 | FDA 510(k) | Class II | Active |
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