KITOTECH MEDICAL INC

FDA Device Registration & Listing · Seattle, WA, US · Registration 3012261738

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3012261738
FEI Number
3012261738
Entity Name
KITOTECH MEDICAL INC
City/State/Country
Seattle, WA, US
Establishment Address
255 S King St, Suite 800, Seattle, WA 98104, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
KitoTech Medical Inc (Owner Number: 10051211)
Owner / Operator Contact Address
255 S King St, Suite 800, Seattle, WA 98104, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

microMend PainPause microMend PainPause PainPause microMend microMend microMend PainPause

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQX Needle, Acupuncture, Single Use General Hospital Class 2 880.5580 2024-04-22
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2016-02-17
GDT Staple, Removable (Skin) General, Plastic Surgery Class 1 878.4760 2016-02-17
LRR First Aid Kit With Drug Unknown Class N N/A 2020-10-30
OHO First Aid Kit Without Drug General, Plastic Surgery Class 1 878.4014 2020-04-29

Official Correspondent

Ronald Berenson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KitoTech Medical Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012261738. Last updated year: 2026. Please use registration number 3012261738 when referencing this establishment in official correspondence.
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