Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005853093

FEI Number

3005853093

Entity Name

Glytec, LLC

City/State/Country

Greenville, SC, US

Establishment Address

220 N Main St, Greenville, SC 29601, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Glytec, LLC (Owner Number: 9090324)

Owner / Operator Contact Address

220 North Main Street, --, Greenville, SC 29601, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K113853

PMA Number

N/A

All Registered Proprietary Names

Glucommander Glucommander G+

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NDC	Calculator, Drug Dose	Anesthesiology	Class 2	868.1890	2017-10-04
NDC	Calculator, Drug Dose	Anesthesiology	Class 2	868.1890	2012-10-23

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Glytec, LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005853093. Last updated year: 2026. Please use registration number 3005853093 when referencing this establishment in official correspondence.