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
2062041802
Device Listing 2062041802
Listing Summary
#
Listing key
2062041802
Premarket submission
K940261
Device
LYNX LOW-SPEED HANDPIECE
Applicant
Mti Precision Products
Product code
EFB
Decision date
1994-12-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
179899
2246821
2246821
MTI PRECISION PRODUCTS
1
N
2026-01-01
131 Birch St Coatesville PA US 19320