Nobelpharma USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nobelpharma USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM FOR PEDIATRIC USE, NOBLEPHARMA WIDE ACCESSORIES, NOBELPHARMA BONE ANCHORED HEARING AID
64
Total
64
Cleared
0
Denied
Nobelpharma USA, Inc. has 64 FDA 510(k) cleared dental devices. Based in Chicago, US.
Historical record: 64 cleared submissions from 1990 to 1999.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nobelpharma USA, Inc.
64 devices
Cleared
Jun 28, 1999
BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM FOR PEDIATRIC USE
Ear, Nose, Throat
221d
Cleared
Sep 06, 1996
NOBLEPHARMA WIDE ACCESSORIES
Dental
77d
Cleared
Aug 09, 1996
NOBELPHARMA BONE ANCHORED HEARING AID
Ear, Nose, Throat
235d
Cleared
Jul 22, 1996
BRANEMARK SYSTEMS MKII SELK-TAPPING FIXTURE
Dental
49d
Cleared
Jul 18, 1996
17 ANGULATED ABUTMENT
Dental
76d
Cleared
Jul 10, 1996
MIRUSCONE ABUTMENT SYSTEM
Dental
68d
Cleared
Jul 10, 1996
CERA ONE ABUTMENT SYSTEM
Dental
68d
Cleared
May 14, 1996
ABUTMENT SELECTION KIT
Dental
90d
Cleared
Jan 30, 1996
ABUTMENT RETRIEVAL KIT
Dental
47d
Cleared
Jan 23, 1996
BALL ATTACHMENT SYSTEM
Dental
62d
Cleared
Oct 03, 1995
BRANEMARK RADIOGRAPHIC DEPTH GUAGE
Dental
74d
Cleared
Sep 27, 1995
BRANEMARK RESTORATIVE INSTRUMENT & COMPONENT TRAY
Dental
44d
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