Is this your brand? Sign in to claim ownership.
Sign in to claim this brandVitalitec International Medizintechnik GmbH
US
Last updated May 23, 2026
What Vitalitec International Medizintechnik GmbH makes
Vitalitec International Medizintechnik GmbH manufactures reusable orthopedic and surgical instruments, including bone punches for orthopedic procedures and spinal rongeurs for spinal surgery. Their portfolio also includes reusable endoscopic and open-surgery electrosurgical tools, such as monopolar and bipolar electrodes and handpieces, as well as rigid optical arthroscopes for minimally invasive joint examinations.
The company’s devices are classified as Class II under regulatory frameworks, with products listed in the FDA’s Unique Device Identification (UDI) database. The manufacturer operates from the United States, adhering to applicable medical device regulations for reusable surgical instruments and endoscopic equipment.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Vitalitec International Medizintechnik GmbH make?
Vitalitec International Medizintechnik GmbH manufactures reusable orthopedic and surgical instruments, including bone punches for orthopedic procedures, spinal rongeurs for spinal surgery, reusable endoscopic electrosurgical electrodes (monopolar), reusable open-surgery electrosurgical handpieces/electrodes (bipolar, single-use), and rigid optical arthroscopes for minimally invasive joint examinations.
Where is Vitalitec International Medizintechnik GmbH based?
Vitalitec International Medizintechnik GmbH operates from the United States, as indicated by the country field in the device data, which specifies US as the location of the manufacturer.
Which regulatory registries list Vitalitec International Medizintechnik GmbH's devices?
The devices manufactured by Vitalitec International Medizintechnik GmbH are listed in the FDA's Unique Device Identification (UDI) database, as explicitly stated in the LISTED IN field of the provided data.
How are Vitalitec International Medizintechnik GmbH's devices classified?
Vitalitec International Medizintechnik GmbH's devices are classified as Class II under regulatory frameworks, as specified in the DEVICE CLASSES field of the device data, which indicates this classification applies to their products.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 328485453
Catalogue (308)
Page 2 of 7| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vitalitec | VK.J901QRS | FDA UDI | Class II | Active |
| Quick Release | VK.J8015QRF | FDA UDI | Class II | Active |
| Quick Release | VK.802RHE | FDA UDI | Class II | Active |
| Quick Release | VK.J1005CTBC | FDA UDI | Class II | Active |
| Quick Release | VK.J805QR90D | FDA UDI | Class II | Active |
| Quick Release | VK.J11045CTS | FDA UDI | Class II | Active |
| Quick Release | VK.J905CTBD | FDA UDI | Class II | Active |
| Quick Release | VK.J902QR | FDA UDI | Class II | Active |
| Vitalitec | VMJ1002QRBC | FDA UDI | Class II | Active |
| Quick Release | VK.J702CT | FDA UDI | Class II | Active |
| Quick Release | VK.J802CTSC | FDA UDI | Class II | Active |
| Quick Relase | VK.J802QRM | FDA UDI | Class II | Active |
| Quick Release | VK.J904CTBC | FDA UDI | Class II | Active |
| Quick Release | VK.J803CVL | FDA UDI | Class II | Active |
| Quick Release | VK.J801CTS | FDA UDI | Class II | Active |
| Quick Release | VK.J1001QR | FDA UDI | Class II | Active |
| Quick Release | VK.J1103CTBC | FDA UDI | Class II | Active |
| Vitalitec | L-552005 | FDA UDI | Class II | Active |
| Quick Release | VK.J801QR90 | FDA UDI | Class II | Active |
| Vitalitec | VK.J901QRBC90 | FDA UDI | Class II | Active |
| Quick Release | VK.J1002CTSC | FDA UDI | Class II | Active |
| Quick Release | VK.J804CVU | FDA UDI | Class II | Active |
| Quick Release | VK.J11025CTS | FDA UDI | Class II | Active |
| Quick Release | VK.J702CTSC | FDA UDI | Class II | Active |
| Quick Release | VK.J703QR90 | FDA UDI | Class II | Active |
| Quick Release | VK.J703QR | FDA UDI | Class II | Active |
| Quick Release | VK.J1005QR | FDA UDI | Class II | Active |
| Quick Release | VK.J1104CTBC | FDA UDI | Class II | Active |
| Quick Release | VK.J806CTBC | FDA UDI | Class II | Active |
| Vitalitec | VK.J902CTD | FDA UDI | Class II | Active |
| Quick Release | VK.J1002QR | FDA UDI | Class II | Active |
| Quick Release | VK.J1002CVUQR | FDA UDI | Class II | Active |
| Quick Release | VK.J904CTS | FDA UDI | Class II | Active |
| Quick Release | VK.J1304CT | FDA UDI | Class II | Active |
| Quick Release | VK.J803QRS | FDA UDI | Class II | Active |
| Quick Release | VK.J706CT | FDA UDI | Class II | Active |
| Vitalitec | L-588350 | FDA UDI | Class II | Active |
| Quick Release | VK.J1105QRS | FDA UDI | Class II | Active |
| Quick Release | VK.J803CT90 | FDA UDI | Class II | Active |
| Quick Release | VK.J1101CT | FDA UDI | Class II | Active |
| Quick Release | VK.J1302CT | FDA UDI | Class II | Active |
| Vitalitec | VK.J703CVLQR | FDA UDI | Class II | Active |
| Quick Release | VK.J804CVUQR | FDA UDI | Class II | Active |
| Vitalitec | VMJ1002QRS | FDA UDI | Class II | Active |
| Quick Release | VK.J704CTS | FDA UDI | Class II | Active |
| Vitalitec | VMJ704QR | FDA UDI | Class II | Active |
| Quick Release | VK.J809CT | FDA UDI | Class II | Active |
| Quick Release | VK.J1103CTBD | FDA UDI | Class II | Active |
| Vitalitec | VK.J1002QRS | FDA UDI | Class II | Active |
| Quick Release | VK.J803CTBD90 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Vitalitec International Medizintechnik GmbH BALGHEIM Baden-Wurttemberg · DE FEI 3003445992