FDA.reportPublic FDA data

PRO-TECH Design & Mfg, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30105310693010531069PRO-TECH Design & Mfg, Inc.1N2026-01-014041 Express Street Arlington TX US 76001
30130239693013023969PRO-TECH Design & Mfg, Inc.1N2026-01-0113719 Borate St Santa Fe Springs CA US 90670

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1631441594654483P990074NATRELLE SALINE BREAST IMPLANTSFWM2000-05-10
1631441369526295P040046NATRELLE HIGHLY COHESIVE SILICONE-FILLED BREAST IMPLANTSFTR2013-02-20
1631441477002376P020056NATRELLE SILICONE-FILLED BREAST IMPLANTSFTR2006-11-17
1631441639296565K172714LipiVageMUU2017-12-08
1631441987258299K120029HEMI PHALANGEAL IMPLANT SURGICAL INSTRUMENT SETKWD2012-02-06
1990461064313883
1631441068114084
1631441092931409
1631441149366115
1631441154075536
1990461154075536
1990461172643193
1631441175619334
1631441235345735
1990461237470453
1990461260449225
1990461279907915
1990461327433457
1631441334111255
1631441373268361
1990461388657769
1990461400411346
1631441400411346
1631441421163927
1990461451731836
1631441484208213
1631441531766498
1631441540080910
1990461572336741
1631441584654767
1631441639296565
1631441701039888
1631441753465680
1990461753465680
1631441792387305
1990461812324069
1990461823201403
1990461863464281
1631441871124314
1631441896388555

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FTR22013-02-20
MUU12017-12-08
KWD12012-02-06
FWM12000-05-10