Interpore Intl. is one of 15071 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Interpore Intl. - FDA 510(k) Cleared Devices
Recent clearances: ULTRACON ULTRAFILTRATOR, PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30L, INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE
25
Total
25
Cleared
0
Denied
Interpore Intl. has 25 FDA 510(k) cleared dental devices. Based in Walker, US.
Historical record: 25 cleared submissions from 1984 to 1998.
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 - Interpore Intl.
25 devices
Cleared
Dec 11, 1998
ULTRACON ULTRAFILTRATOR
Gastroenterology & Urology
249d
Cleared
Sep 25, 1998
PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05,...
Orthopedic
206d
Cleared
Oct 30, 1997
INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE
Dental
90d
Cleared
Jun 03, 1997
ODONTIT AUTOGENOUS BONE COLLECTION DEVICE
General & Plastic Surgery
75d
Cleared
May 24, 1996
IMZ MEMBRANE TACK SYSTEM
Dental
77d
Cleared
Mar 08, 1996
INTERPORE THREADED IMPLANT
Dental
42d
Cleared
Jan 30, 1996
INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLT
Dental
60d
Cleared
Nov 21, 1995
IMZ BONE TACK SYSTEM
Dental
197d
Cleared
Mar 28, 1995
INTERPORE IP 200 GRANULAR CORALLINE HYDROXYAPATITE BONE VOID FILLERS, 425 TO...
Dental
70d
Cleared
Jul 25, 1994
INTERPORE CYLINDRICAL HEX HYDROXYAPATITE COATED IMPLANT, 3.3 MM DIAM.
Dental
770d
Cleared
Feb 10, 1994
INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER
Dental
612d
Cleared
Oct 13, 1992
INTERPORE IMZ CYLINDER IMPLANT SYSTEM
Dental
449d