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I will register your fda medical device establishment and device listing
About this Gig
Are you planning to manufacture, import, distribute, relabel, or repackage medical devices in the United States?
I will assist your company with FDA Medical Device Establishment Registration and Device Listing to help meet FDA regulatory requirements.
Whether you are a medical device manufacturer, specification developer, contract manufacturer, repackager, relabeler, or importer, I can guide you through the registration and listing process and help ensure that all required information is properly prepared and submitted.
My Services Include:
FDA Medical Device Establishment Registration
FDA Device Listing Assistance
Owner/Operator Account Setup
FDA FURLS Account Assistance
U.S. Agent Information Guidance (for foreign manufacturers)
FDA Registration Renewal Support
Device Classification Research
FDA Regulatory Compliance Consultation
Importer and Initial Distributor Registration Guidance
Assistance with FDA Correspondence
Industries Served:
- Medical Devices
- Diagnostic Devices
- Surgical Instruments
- Dental Devices
- Orthopedic Devices
- Laboratory Equipment
- Healthcare Products
Why Choose Me?
- Professional FDA Regulatory Support
- Fast Response Time
- Accurate Documentation Review
- Experience with
Field of law:
Business (corporate)
Target country:
United States
Document type:
Disclaimer
•
Estate planning
•
DMCA claims
Legal consulting Gigs are not screened
Please note that there is no screening process for this service. We recommend that you message the freelancer and check all necessary details before placing your order. Pro freelancers in this category have gone through a vetting process. You can find more details here.
FAQ
Do FDA medical device companies need establishment registration?
Yes. Most companies involved in manufacturing, importing, relabeling, repackaging, or distributing medical devices in the U.S. must register their establishments with the FDA and list their devices unless exempt.
Can you guarantee FDA approval?
No. Establishment registration and device listing are administrative FDA requirements and do not constitute FDA approval or clearance.
Do foreign manufacturers need a U.S. Agent?
Yes. Foreign medical device establishments generally must designate a U.S. Agent when registering with the FDA.
Can you help determine my device classification?
Yes. I can conduct device classification research and identify potential FDA product codes
Is device listing the same as a 510(k)?
No. Device listing is different from a 510(k) submission. Some devices require 510(k) clearance before marketing, while others may be exempt.
Do I need to renew FDA registration every year?
Yes. FDA establishment registration generally requires annual renewal during the FDA registration period.
