# Austenal Dental, Inc.

- Location (FDA's records): Chicago, IL
- FDA decisions: 19 (1985–1989): 19 510(k) clearances
- Product codes: EJH (6), EBI (5), EJS (2), EKG (1), DZE (1), ELW (1), ELM (1), EJW (1), EBD (1)
- Predicates its devices cite: 0 (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 that cite its devices most
- Austenal, Inc.: 1 (https://510kreport.com/company/austenal)

## Its most-cited devices
- K880875: Vitallium Equipoise Alloy (1988), cited by 1

## Recent decisions
- K890713: Overdenture - Stud Attachment (Jul 14, 1989)
- K883799: Base, Denture, Relining, Repairing, Rebasing,Resin (Oct 20, 1988)
- K880875: Vitallium Equipoise Alloy (Apr 7, 1988)
- K871849: Light Cure Denture Glaze (Aug 10, 1987)
- K872746: Vitallium Wire (Jul 21, 1987)
- K863630: Austenal Acupac 20 Denture Base Material (Mar 11, 1987)
- K865025: Austenal Condensing Instrument (Feb 19, 1987)
- K862557: Austenal Acusoft Soft Liner (Feb 19, 1987)

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