Medical Device Manufacturer · US , Mchenry , IL

Deringer-Ney, Inc. - FDA 510(k) Cleared Devices

46 submissions · 46 cleared · Since 1976

Recent clearances: GDC 3509, DENTAL CASTING ALLOY MODIFICATION-PF-4, DENTAL CASTING ALLOY, MODIFICATION - PF-3

Total

Cleared

Denied

Deringer-Ney, Inc. has 46 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 46 cleared submissions from 1976 to 1993.

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

Deringer-Ney, 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 - Deringer-Ney, Inc.

46 devices

1-12 of 46

DENTAL CASTING ALLOY MODIFICATION-PF-4

K930481 · EJT

Dental · 61d

Cleared Mar 31, 1993

DENTAL CASTING ALLOY, MODIFICATION - PF-3

GDC-3338, DENTAL SOLDER ALLOY

K920887 · EJS

Dental · 77d

Cleared Mar 15, 1991

GDC-3200 DENTAL SOLDER

GDC 3084 CASTING ALLOY

K901532 · EJT

Dental · 30d

Cleared Dec 20, 1989

SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL)

K893800 · EJT

Dental · 212d

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Deringer-Ney, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Deringer-Ney, Inc.

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