Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1209089233
Device Listing 1209089233
Listing Summary
#
Listing key
1209089233
Premarket submission
K902489
Device
MODIFIED MOLTENO(TM) IMPLANTS
Applicant
Iop, Inc.
Product code
KYF
Decision date
1990-08-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
36213
2242450
2242450
KATENA PRODUCTS, INC.
1
Y
2026-01-01
4 Middlebury Boulevard Unit #1 Randolph NJ US 07869
224205
3015177648
3015177648
KATENA PRODUCTS, INC.
1
Y
2026-01-01
6 CAMPUS DRIVE SUITE 310 Parsippany NJ US 07054