# Kendall Research Center

- Location (FDA's records): Mchenry, IL
- FDA decisions: 14 (1976–1980): 14 510(k) clearances
- Product codes: NAB (3), CAZ (2), EZL (1), ITG (1), FQM (1), JOW (1), FFG (1), KOA (1), GDY (1), FCN (1), GBX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 2 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Sterilmed, Inc.: 1 (https://510kreport.com/company/sterilmed)
- Tyco Healthcare/Kendall: 1 (https://510kreport.com/company/tyco-healthcare-kendall)
- Covidien: 1 (https://510kreport.com/company/covidien)
- Vanguard Medical Concepts, Inc.: 1 (https://510kreport.com/company/vanguard-medical-concepts)
- Tyco Healthcare: 1 (https://510kreport.com/company/tyco-healthcare)

## Its most-cited devices
- K781357: T.E.D. Sequential Compression Sleeves (1978), cited by 5

## Recent decisions
- K802225: Tender-Sorb Drain Sponges (Sep 26, 1980)
- K781357: T.E.D. Sequential Compression Sleeves (Sep 20, 1978)
- K780408: Micronet Light Dressing Sponge (Mar 22, 1978)
- K780062: Catheter/Hemostatic/Geriatric (Feb 14, 1978)
- K780120: Anesthesia Tray, Caudal (Feb 6, 1978)
- K772134: Syringe, Irrigation, Pre-Filled (Nov 28, 1977)
- K772133: Urine Specimen Collecting Device (Nov 28, 1977)
- K771655: Curity Peakometer (Oct 14, 1977)

Source page: https://510kreport.com/company/kendall-research-center