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Sign in to claim this brandPeter Lazic GmbH
US
Last updated May 27, 2026
What Peter Lazic GmbH makes
Peter Lazic GmbH manufactures reusable surgical instruments for neurosurgery and open surgery, including aneurysm clips, aneurysm clip appliers, neurosurgical scissors, spinal rongeurs, dissectors, bipolar electrosurgical handpieces, soft-tissue manipulation forceps, and non-illuminating suction cannulae.
The company’s products are classified as Class I and Class II devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. 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 Peter Lazic GmbH manufacture?
Peter Lazic GmbH specializes in reusable surgical instruments primarily used in neurosurgery and open surgery. Their product lineup includes aneurysm clips and appliers, neurosurgical scissors, spinal rongeurs, open-surgery dissectors, bipolar electrosurgical handpieces, soft-tissue manipulation forceps, and non-illuminating suction cannulae. These instruments are designed for precision and durability in critical surgical procedures.
Where is Peter Lazic GmbH based?
Peter Lazic GmbH is headquartered in the United States. The company’s location in the US aligns with regulatory requirements for manufacturing and distributing medical devices in North America, ensuring compliance with local and international standards.
Which regulatory registries list Peter Lazic GmbH’s devices?
Peter Lazic GmbH’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices under FDA oversight, ensuring transparency and traceability for healthcare providers and regulators.
How are Peter Lazic GmbH’s devices classified under FDA regulations?
Peter Lazic GmbH’s devices are classified as either Class I or Class II under FDA regulations. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional performance standards or special controls due to moderate risk. The classification depends on the device’s intended use and potential impact on patient safety.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- peterlazic.com
- —
- —
- [email protected]
- Phone
- 1 844 261 3271
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 327681359
Catalogue (2292)
Page 46 of 46| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Lazic | 70.032.04 | FDA UDI | Class I | Active |
| Lazic | 46.711.22 | FDA UDI | Class I | Active |
| Lazic | 74.773.25 | FDA UDI | Class I | Active |
| Lazic | S.35.740 | FDA UDI | Class II | Active |
| Lazic | 70.151.21 | FDA UDI | Class II | Active |
| Lazic | 74.474.33 | FDA UDI | Class I | Active |
| Lazic | S.45.763 | FDA UDI | Class II | Active |
| Lazic | 65.389 T | FDA UDI | Class II | Active |
| Lazic | 46.943.04 | FDA UDI | Class I | Active |
| Lazic | 65.523 | FDA UDI | Class II | Active |
| Lazic | S.45.822 | FDA UDI | Class II | Active |
| Lazic | 46.363.02 | FDA UDI | Class I | Active |
| Lazic | 45.858 | FDA UDI | Class II | Active |
| Lazic | 46.378.02 T | FDA UDI | Class I | Active |
| Lazic | 65.540 | FDA UDI | Class II | Active |
| Lazic | 74.355.00 | FDA UDI | Class I | Active |
| Lazic | 70.059.04 | FDA UDI | Class I | Active |
| Lazic | 70.126.02 B | FDA UDI | Class I | Active |
| Lazic | 70.153.03 B | FDA UDI | Class I | Active |
| Lazic | 74.473.32 | FDA UDI | Class I | Active |
| Lazic | 69.243.21 | FDA UDI | Class II | Active |
| Lazic | 74.773.34 B | FDA UDI | Class I | Active |
| Lazic | 69.423.21 | FDA UDI | Class II | Active |
| Lazic | 64.404.21 | FDA UDI | Class I | Active |
| Lazic | 46.371.02 T | FDA UDI | Class I | Active |
| Lazic | 70.122.04 B | FDA UDI | Class I | Active |
| Lazic | 45.351 | FDA UDI | Class II | Active |
| Lazic | 45.410 S | FDA UDI | Class II | Active |
| Lazic | 64.825.03 | FDA UDI | Class I | Active |
| Lazic | 70.147.02 | FDA UDI | Class I | Active |
| Lazic | 65.8211 | FDA UDI | Class II | Active |
| Lazic | 46.361.02 | FDA UDI | Class I | Active |
| Lazic | 65.8291 TI | FDA UDI | Class II | Active |
| Lazic | 65.532 T | FDA UDI | Class II | Active |
| Lazic | 45.819 | FDA UDI | Class II | Active |
| Lazic | S.35.710 | FDA UDI | Class II | Active |
| Lazic | 30.613.20 | FDA UDI | Class I | Active |
| Lazic | 46.303 | FDA UDI | Class I | Active |
| Lazic | 30.601.20 | FDA UDI | Class I | Active |
| Lazic | 45.748 | FDA UDI | Class II | Active |
| D-Clip; D-Clip Applier | K180757 | FDA 510(k) | Class II | Active |
| L-Aneurysm-Clip System & L-Aneurysm Clip Appliers, Yasargil Aneurysm Clips & Yasargil Aneurysm Clip Appliers | K081489 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Peter Lazic Gmbh TUTTLINGEN Baden-Wurttemberg · DE FEI 3007264034