RISKWISE SUPPLIES LLC

FDA Device Registration & Listing · Lorton, VA, US · Registration 3041850200

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
3041850200
FEI Number
3041850200
Entity Name
RISKWISE SUPPLIES LLC
City/State/Country
Lorton, VA, US
Establishment Address
9127 Kevin Kraig Rd, Lorton, VA 22079, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
RiskWise Supplies LLC (Owner Number: 10094212)
Owner / Operator Contact Address
9127 Kevin Kraig Rd., Lorton, VA 22079, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Respiratory Shield Travel Kit – Individual Respiratory Shield Travel Kit – Family

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MSH Respirator, Surgical General, Plastic Surgery Class 2 878.4040 2025-11-19

Official Correspondent

Katherine Kinder

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RiskWise Supplies LLC
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
K102092 Prestige Ameritech PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES 2010-10-06

Similar Registrations

Registration Number Establishment Name Location
3020623413 NITTA S.A. Bogota, CO
3016765490 XIAMEN CHUANFUTANG PHARMACEUTICAL CO.,LTD xiamen Fujian, CN
3018382937 MID-AMERICA SAFETY CORP Elk Grove Village, IL, US
3010141571 Xiantao Zhongyi Safety & Protection Products Co.,Ltd. Xiantao City Hubei, CN
3010375076 Shandong Chengsheng Healthcare Products co.,Ltd Weifang Shandong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3041850200. Last updated year: 2026. Please use registration number 3041850200 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.