Medical Device Manufacturer · US , Chicago , IL

Austenal, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1992

Total

Cleared

Denied

Austenal, Inc. has 10 FDA 510(k) cleared dental devices. Based in Chicago, US.

Historical record: 10 cleared submissions from 1992 to 2001.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Austenal, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Austenal, Inc.

10 devices

1-10 of 10

MYERSON'S ECONOMY DENTURE BASE MATERIAL

MIDAS GOLD ELECTROFORMING SYSTEM

K955509 · EJT

Dental · 24d

Cleared Nov 29, 1995

MYERSON IR DENTURE BASE

K954810 · EBI

Dental · 41d

Cleared Jan 05, 1994

MYERSON'S PERMASOFT SOFT RELINE MATERIAL

K933468 · EBI

Dental · 173d

Cleared Nov 04, 1992

DENTURE PLASTIC TEETH

K924526 · ELM

Dental · 57d

Austenal, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Austenal, Inc.

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