CRE-MED

FDA Device Registration & Listing · Albuquerque, NM, US · Registration 3010057648

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
3010057648
FEI Number
3010057648
Entity Name
CRE-MED
City/State/Country
Albuquerque, NM, US
Establishment Address
4101 Masthead St NE, Albuquerque, NM 87109, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
CRE-MED (Owner Number: 10042728)
Owner / Operator Contact Address
4101 Masthead St. NE, Albuquerque, NM 87109, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Kinesio Tex Gold FP Wave

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2012-12-21

Official Correspondent

Shannon Phillips

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CRE-MED
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 3010057648. Last updated year: 2026. Please use registration number 3010057648 when referencing this establishment in official correspondence.
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