NeedleTech Products, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30062833193006283319NeedleTech Products, Inc.1N2026-01-01452 John L Dietsch Blvd N Attleboro MA US 02763

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
977061819268843K143252Galt Tork, 0.010 to 0.020 inches (yellow), Galt Tork, 0.025 to 0.040 inches (orange)DQX2015-04-23
977061095623937K121337UROPLASTY RIGID ENDOSCPIC NEEDLESFBK2012-08-03
977061396377858K102566OWL CANNULAEGXI2011-06-03
977061765455444K090955SMITH & NEPHEW RF CANNULATEGXI2009-07-16
977061116413157K031173NEEDLETECH GUIDEWIRE INTRODUCER NEEDLE, MODELS 40021, 40069, 40053, 40042 & 40013GDF2003-07-23
977061308731423
977061676122849
977061984162740
977062025304554
977061082378099
977061108758527
977061169200985
977061362941065
977061465743914
977061590264666
977061700306330
977061855815254
977061857821467

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GXI22011-06-03
DQX12015-04-23
FBK12012-08-03
GDF12003-07-23

PMN#