# Austenal, Inc.

- Location (FDA's records): Chicago, IL
- FDA decisions: 10 (1992–2001): 10 510(k) clearances
- Product codes: EBI (3), EIH (2), EJH (2), EJT (1), EBF (1), ELM (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 9 (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
- Austenal Dental, Inc.: 1 (https://510kreport.com/company/austenal-dental)

## Firms that cite its devices most
- Roydent Dental Products, Inc.: 1 (https://510kreport.com/company/roydent-dental-products)
- Kavo America: 1 (https://510kreport.com/company/kavo-america)
- Dentsply Intl.: 1 (https://510kreport.com/company/dentsply-intl)
- Nano-Write Corp.: 1 (https://510kreport.com/company/nano-write)
- Tokuyama Dental Corporation: 1 (https://510kreport.com/company/tokuyama-dental)
- New Stetic: 1 (https://510kreport.com/company/new-stetic)
- Cerasys, Inc.: 1 (https://510kreport.com/company/cerasys)
- Oratio B.V.: 1 (https://510kreport.com/company/oratio)

## Its most-cited devices
- K001815: DC Zirkon (2000), cited by 3
- K933468: Myerson's Permasoft Soft Reline Material (1994), cited by 2
- K970522: Myerson's Economy Denture Base Material (1997), cited by 1
- K001798: DC Titan (2000), cited by 1
- K001799: DC-Tell (2000), cited by 1
- K954810: Myerson IR Denture Base (1995), cited by 1

## Recent decisions
- K011674: DC - Cristal (Sep 4, 2001)
- K001799: DC-Tell (Aug 10, 2000)
- K001815: DC Zirkon (Aug 10, 2000)
- K001798: DC Titan (Jul 31, 2000)
- K970522: Myerson's Economy Denture Base Material (May 14, 1997)
- K970205: Vitallium 2000 Alloy; Vitallium 2000 Plus Alloy; Cobalt Chrome Casting Alloy (Apr 21, 1997)
- K955509: Midas Gold Electroforming System (Dec 28, 1995)
- K954810: Myerson IR Denture Base (Nov 29, 1995)

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