# Turnkey Intergration USA, Inc.

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 26 (1990–1999): 26 510(k) clearances
- Product codes: LWJ (3), LZO (3), HRS (2), KWA (2), JDI (2), KTW (2), JWI (1), LZN (1), KWY (1), JDG (1), LPH (1), HSD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Fournitures Hospitalieres: 2 (https://510kreport.com/company/fournitures-hospitalieres)
- Ferguson Medical: 1 (https://510kreport.com/company/ferguson-medical)
- Newclip Technics: 1 (https://510kreport.com/company/newclip-technics)
- Acu Med, Inc.: 1 (https://510kreport.com/company/acu-med)
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)

## Its most-cited devices
- K912936: May Humerus Plates (1991), cited by 3
- K923911: Intrinsic Stem (1993), cited by 2
- K913282: Lima RPS Shoulder (1991), cited by 1

## Recent decisions
- K991405: Omni-Fix, Humeral Nail (Jun 29, 1999)
- K990523: B2C, Espace Revision Cup System (Apr 30, 1999)
- K990307: Omni-Fix, Nail System (Apr 1, 1999)
- K972411: Link Cement Plug (Aug 29, 1997)
- K970284: Artos, Diplos System (Apr 21, 1997)
- K970084: Link Cerclage Wire System (Mar 13, 1997)
- K953653: Lubinus SP II Hip System (Nov 6, 1995)
- K943986: Link Endo Model Revision Cup (Jul 5, 1995)

Source page: https://510kreport.com/company/turnkey-intergration-usa