FDA.reportPublic FDA data

HARBOR MEDTECH, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30100971293010097129HARBOR MEDTECH, INC.1N2026-01-0121076 Bake Parkway Suite 100 Lake Forest CA US 92630

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00854780005409Architect Fx - Collagen Wound Matrix(888) 346-9802complaints@stimlabs.com
00854780005447Architect Fx - Collagen Wound Matrix(888) 346-9802complaints@stimlabs.com
00854780005454Architect Fx - Collagen Wound Matrix(888) 346-9802complaints@stimlabs.com
00854780005461Architect Fx - Collagen Wound Matrix(888) 346-9802complaints@stimlabs.com
00854780005478Architect Fx - Collagen Wound Matrix(888) 346-9802complaints@stimlabs.com
00854780005485Architect Fx - Collagen Wound Matrix(888) 346-9802complaints@stimlabs.com
00854780005492Architect Fx - Collagen Wound Matrix(888) 346-9802complaints@stimlabs.com
00854780005515Architect Fx - Collagen Wound Matrix(888) 346-9802complaints@stimlabs.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3289571517251615K140367ARCHITECT PX EXTRACELLULAR COLLAGEN MATRIXKGN2014-09-12
3289571266415480K122502BRIDGE EXTRACELLULAR COLLEGEN MATRIXKGN2013-02-26

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KGN22014-09-12

PMN#

GUDID#

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