# Specialized Health Products International, Inc.

- Location (FDA's records): Salt Lake, UT
- FDA decisions: 2 (2007–2008): 2 510(k) clearances
- Product codes: KNT (1), FPA (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Specialized Health Products, Inc.: 1 (https://510kreport.com/company/specialized-health-products)
- Teleflex Medical: 1 (https://510kreport.com/company/teleflex-medical)
- Luther Needlesafe Products, Inc.: 1 (https://510kreport.com/company/luther-needlesafe-products)
- Luther Research Partners: 1 (https://510kreport.com/company/luther-research-partners)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Rita Medical Systems: 1 (https://510kreport.com/company/rita-medical-systems)
- Smiths Medical MD, Inc.: 1 (https://510kreport.com/company/smiths-medical-md)

## Firms that cite its devices most
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Aspire Bariatrics, Inc.: 1 (https://510kreport.com/company/aspire-bariatrics)
- Mps Acacia: 1 (https://510kreport.com/company/mps-acacia)
- B.Braun Medical, Inc.: 1 (https://510kreport.com/company/b-braun-medical)

## Its most-cited devices
- K073050: Safestep Max Power-Injectable Infusion Set (2008), cited by 3
- K070449: Lumiloc (TM) Safety Introducer Needle (2007), cited by 1

## Recent decisions
- K073050: Safestep Max Power-Injectable Infusion Set (Jan 25, 2008)
- K070449: Lumiloc (TM) Safety Introducer Needle (Jun 14, 2007)

Source page: https://510kreport.com/company/specialized-health-products-international