FDA.reportPublic FDA data

ORTHO PRECISION PRODUCTS

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30110530363011053036ORTHO PRECISION PRODUCTS1N2026-01-013201 W. El Segundo Blvd Hawthorne CA US 90250

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1740831820919431K153338Tiger Cannulated Screw SystemHWC2016-01-14
1740831772666925K120148AOS SOLID LOCKING LAG SCREW, AOS TELESCOPING LAG SCREWHSB2012-10-02
1740831266065084K112737TIGER HEADLESS CANNULATED SCREWSHWC2011-10-20
1740831384868706K103533ES TROCHANTERIC NAIL, LEFT AND RIGHT, 10MMHSB2011-01-19
1740831475065183K070444AOS TIBIAL NAILHSB2007-06-14
1740831248506222K050241AOS HUMERAL NAILHSB2005-03-14
1740831101941256K021008ADVANCED ORTHOPAEDIC SOLUTIONS TROCHANTERIC NAILHSB2002-06-20
1740831618147969K012190AOS MODULAR FEMORAL NAILHSB2001-09-24

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
HSB62012-10-02
HWC22016-01-14