# Obtech Medical GmbH

- Location (FDA's records): Zug
- FDA decisions: 2 (2007–2007): 1 510(k) clearance and 1 original PMA approval
- Names in FDA's records: Obtech Medical GmbH (1); Obtech Medical Sarl (1)
- Product codes: LTI (1), KNT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 19 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Covidien: 1 (https://510kreport.com/company/covidien)
- Medical Innovation Development: 1 (https://510kreport.com/company/medical-innovation-development)
- Boehringer Laboratories: 1 (https://510kreport.com/company/boehringer-laboratories)

## Its most-cited devices
- K071764: Realize Gastric Calibration Tube, Models GCT180, GCT360 (2007), cited by 3

## Recent decisions
- K071764: Realize Gastric Calibration Tube, Models GCT180, GCT360 (Oct 24, 2007)
- P070009: Realize Adjustable Gastric Band Model 2200-X (Sep 28, 2007)

Source page: https://510kreport.com/company/obtech-medical