# Tekka

- Location (FDA's records): Bethesda, MD
- FDA decisions: 2 (2003–2003): 2 510(k) clearances
- Product codes: JEY (2)
- Predicates its devices cite: 13 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Walter Lorenz Surgical, Inc.: 4 (https://510kreport.com/company/walter-lorenz-surgical)
- KLS-Martin L.P.: 3 (https://510kreport.com/company/kls-martin)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Stryker Instruments: 2 (https://510kreport.com/company/stryker-instruments)
- Osteomed LP: 1 (https://510kreport.com/company/osteomed)
- Bioplate, Inc.: 1 (https://510kreport.com/company/bioplate)

## Firms that cite its devices most
- Frontier Devices, Inc.: 1 (https://510kreport.com/company/frontier-devices)

## Its most-cited devices
- K031989: Ortrautek Orthognathic System (2003), cited by 1

## Recent decisions
- K032520: Ortrautek Trauma System (Nov 12, 2003)
- K031989: Ortrautek Orthognathic System (Oct 28, 2003)

Source page: https://510kreport.com/company/tekka