BIOTECH, INC.

FDA Device Registration & Listing · Alpharetta, GA, US · Registration 3010781586

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
3010781586
FEI Number
3010781586
Entity Name
BIOTECH, INC.
City/State/Country
Alpharetta, GA, US
Establishment Address
5975 Shiloh Rd Ste 101, Alpharetta, GA 30005, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Biotech, Inc. (Owner Number: 10046047)
Owner / Operator Contact Address
5975 Shiloh Road, Suite 101, Alpharetta, GA 30005, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

CRYOLOCK

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQK Labware, Assisted Reproduction Obstetrics/Gynecology Class 2 884.6160 2014-01-27

Official Correspondent

Jorge Parra

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Biotech, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010781586. Last updated year: 2026. Please use registration number 3010781586 when referencing this establishment in official correspondence.
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