Snowrock USA

FDA Device Registration & Listing · Buford, GA, US · Registration 3010368334

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
3010368334
FEI Number
3010368334
Entity Name
Snowrock USA
City/State/Country
Buford, GA, US
Establishment Address
4195 S Lee St Ste K, Buford, GA 30518, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Snowrock USA (Owner Number: 10045607)
Owner / Operator Contact Address
3145 Reps Miller Rd., Suite A, Norcross, GA 30071, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Snow Rock Snow Rock Snow Rock

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JES Floss, Dental Dental Class 1 872.6390 2013-12-06
EBI Resin, Denture, Relining, Repairing, Rebasing Dental Class 2 872.3760 2013-12-06
JEW Tip, Rubber, Oral Hygiene Dental Class 1 872.6650 2013-12-06

Official Correspondent

Brian Kim

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Snowrock USA
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
K882164 Arthur Blank & Co., Inc. FLOSS CARD 1988-06-10
K800400 Dentsply Intl. MAXUM DENTURE RESIN 1980-03-12
K033020 Cmp Industries, LLC IMPAK ACRYLIC REPAIR RESIN LIQUID 2003-12-19

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010368334. Last updated year: 2026. Please use registration number 3010368334 when referencing this establishment in official correspondence.
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