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Sign in to claim this brandAckermann Instrumente GmbH
US
Last updated May 24, 2026
What Ackermann Instrumente GmbH makes
The company produces reusable endoscopic electrosurgical handpieces and electrodes for monopolar procedures, as well as reusable laparoscopic access cannulas for minimally invasive surgery. It also manufactures metallic ligation clips and appliers, including endoscopic versions, alongside reusable suturing needle holders for precise tissue manipulation. The portfolio includes aneurysm clip appliers for vascular procedures and a range of reusable clip appliers designed for secure tissue ligation.
The devices fall under FDA classifications of Class I and Class II, with regulatory submissions including 510(k) clearances and entries in the FDA’s Unique Device Identifier (UDI) database. The company’s products are listed under these regulatory pathways in the United States, where the manufacturer is based.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- ackermanninstrumente.de
- —
- —
- [email protected]
- Phone
- +497461966170
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 315121009
Catalogue (112)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Seculock | 13-1346SQI | FDA UDI | Class II | Active |
| Seculock | 13-1302SQI | FDA UDI | Class II | Active |
| Seculock | 13-1324SQI | FDA UDI | Class II | Active |
| Seculock | 13-1377SQI | FDA UDI | Class II | Active |
| Endolock | 13-1300I | FDA UDI | Class II | Active |
| Seculock | 13-1309SQI | FDA UDI | Class II | Active |
| Seculock | 13-1304SQI | FDA UDI | Class II | Active |
| Seculock | 13-1315SQI | FDA UDI | Class II | Active |
| Eth Needle Holder | 13-1594ET | FDA UDI | Class I | Active |
| Ackermann Surgical Instruments | K974382 | FDA 510(k) | Class II | Active |
| Ackermann Europclip | K111930 | FDA 510(k) | Class II | Active |
| Ackermann Intervertebral Body Fusion Device | K143450 | FDA 510(k) | Class II | Active |
Related Companies
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Authorities
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Ackermann Instrumente Gmbh RIETHEIM, WEILHEIM Baden-Wurttemberg · DE FEI 4486