Medical Device Manufacturer · US , Newtown , PA

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

24 submissions · 24 cleared · Since 1991

Recent clearances: REMATITAN TITANIUM, REMANIUM:GM 700, GM 380, GM 800, GFH, REMANIUM: CS & G-SOFT

Total

Cleared

Denied

Dentauraum, Inc. has 24 FDA 510(k) cleared dental devices. Based in Newtown, US.

Historical record: 24 cleared submissions from 1991 to 1995.

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

Dentauraum, 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 - Dentauraum, Inc.

24 devices

1-12 of 24

REMANIUM:GM 700, GM 380, GM 800, GFH

K952867 · EJH

Dental · 35d

Cleared Jul 27, 1995

REMANIUM: CS & G-SOFT

K952870 · EJH

Dental · 35d

Cleared Jul 26, 1995

REMANIUM: 200,CS, 380, AND CD

K952865 · EJH

Dental · 34d

Cleared Jul 19, 1995

DENTAURUM JACKET CROWN & ROOT POSTS

K952868 · EBL

Dental · 27d

Cleared Feb 13, 1995

DENT-O-CRYL ORTHODONTIC ACRYLIC

K942667 · KMY

Dental · 252d

Cleared Aug 10, 1994

ORTHALGENAT IMPRESSION MATERIAL

ORTHOCENT: LIQUID AND POWDER

K942665 · EMA

Dental · 46d

Cleared Jul 22, 1994

O-TRAY IMPRESSION TRAYS

K942668 · EHY

Dental · 46d

Cleared Apr 28, 1994

DENTAURUM SPACE MAINTAINER

K935856 · DYT

Dental · 141d

Cleared Feb 04, 1994

FASCINATION CERAMIC BRACKET

K935139 · EJF

Dental · 99d

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

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

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