Ackermann Instrumente GmbH
US Last updated 24 May 2026
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- Devices
- 112
- Registries
- GUDIDFDA
- FDA recalls
- 0
Catalogue
Eth Needle Holder 13-1593ET Ref 13-1593ET
Seculock 13-1313SQI Ref 13-1313SQI
Seculock 13-1333SQI Ref 13-1333SQI
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Europclip Ai-321528DD Ref AI-321528DD
Europclip Ai-321536DD Ref AI-321536DD
Seculock 13-1340SQI Ref 13-1340SQI
Seculock 13-1320SQI Ref 13-1320SQI
Seculock 13-1327SQI Ref 13-1327SQI
Endolock 13-0530I Ref 13-0530I
Eth Needle Holder 13-1591ET-45 Ref 13-1591ET-45
Seculock 13-1382SQI Ref 13-1382SQI
Seculock 13-1378SQI Ref 13-1378SQI
Seculock 13-1375SQI Ref 13-1375SQI
Endolock 13-1301I Ref 13-1301I
Europclip Ai-321532DD Ref AI-321532DD
Seculock 13-1306SQI Ref 13-1306SQI
Europclip Ai-321550DD Ref AI-321550DD
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Europclip AI74CL6 Ref AI74CL6
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Seculock 13-1360SQ Ref 13-1360SQ
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Europclip Ai-321544DD Ref AI-321544DD
Europclip Ai-321552DD Ref AI-321552DD
Seculock 13-1354SQI Ref 13-1354SQI
Seculock 13-1331SQI Ref 13-1331SQI
Seculock 13-1348SQI Ref 13-1348SQI
Europclip AI74CL6 Ref AI74CL6
Seculock 13-1380SQI Ref 13-1380SQI
Seculock 13-1326SQI Ref 13-1326SQI
Europclip AI74CML6 Ref AI74CML6
Europclip Ai-321534DD Ref AI-321534DD
Ackermann Trockar Sleeve 10-1117THC Ref 10-1117THC
Seculock 13-1321SQI Ref 13-1321SQI
Seculock 13-1303SQI Ref 13-1303SQI
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Seculock 13-1338SQI Ref 13-1338SQI
Seculock 13-1341SQI Ref 13-1341SQI
Seculock 13-1356SQ Ref 13-1356SQ
EUROPCLIP Applier 13-1613-106AS Ref 13-1613-106AS
Showing 1-50 of 112
FDA establishments
- Ackermann Instrumente GmbH RIETHEIM, WEILHEIM Baden-Wurttemberg · DE FEI 4486
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.
Information
- Country
- US
- Website
- ackermanninstrumente.de
- [email protected]
- Phone
- +497461966170
- DUNS number
- 315121009