DESIGN STANDARDS CORP.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
12222741000121057DESIGN STANDARDS CORP.1N2026-01-01957 Claremont Rd CHARLESTOWN NH US 03603

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
14681718595478K113706ENDOWRIST STAPLER SYSTEMNAY2012-10-17
14681471267350K103412AXIOM FASCIAL CLOSURE SYSTEMOCW2010-12-30
14681253783493K091697SPIDER SURGICAL INSTRUMENTS, MODELS 90004, 90005, 90007, 90009, 90010, 90012, 90013, 90015GCJ2009-09-28
14681100858560
14681482515993
14681683651992
14681727365401
14681023071179
14681081854412
14681112134589
14681137465618
14681166935869
14681170593359
14681191442176
14681225498548
14681359730523
14681382909597
14681385324679
14681414693174
14681581908701
14681607642932
14681656362482
14681709392295
14681736793816
14681766777457
14681790284900
14681812718266
14681821821798
14681849173166
14681859687714
14681868923217
14681895533353
14681958255895
14681968774921
14681991187499

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NAY12012-10-17
OCW12010-12-30
GCJ12009-09-28

PMN#

GUDID#