• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
1 to 10 of 23 Results
ProductCode: DZE Applicant: LIFECORE BIOMEDICAL, INC. Decision Date To: 11/26/2022
 
 1 
 2 
 3 
 > 
Results per Page
New Search  
Export all 23 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
restore, stage-1, renova primasolo and primaconnex dental implants LIFECORE BIOMEDICAL, INC. K072768 10/23/2007
primaconnex internal connection implant system, primaconnex internal connection prosthetics LIFECORE BIOMEDICAL, INC. K051614 09/09/2005
primasolo one-piece implants & healing caps LIFECORE BIOMEDICAL, INC. K050506 04/15/2005
renova internal hex implant system LIFECORE BIOMEDICAL, INC. K032774 11/26/2003
the lifecore stage-1 angled abutment system LIFECORE BIOMEDICAL, INC. K032495 09/17/2003
lifecore biomedical dental implant systems LIFECORE BIOMEDICAL, INC. K002037 05/16/2001
the lifecore stage-1 single stage rbm dental implant system LIFECORE BIOMEDICAL, INC. K003226 01/12/2001
lifecore single tooth abutment system LIFECORE BIOMEDICAL, INC. K993894 03/08/2000
modification of regular diameter single stage (rds) tps dental implant system LIFECORE BIOMEDICAL, INC. K994205 02/29/2000
regular diameter single stage (rds) tps dental implant system LIFECORE BIOMEDICAL, INC. K991114 07/14/1999
-
-