FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Acid, Hyaluronic, Intraarticular

PMA: P080020 · Supplement: S054 · Decision Jun 18, 2025
Classifications
1
FEI Numbers
21
Registration Numbers
21

Basic Information

Device Name
Acid, Hyaluronic, Intraarticular
Trade Name
Gel-One
PMA Number
P080020
Supplement Number
S054
Device Class
FDA Class 3
Product Code
MOZ
Generic Name
Acid, hyaluronic, intraarticular
Medical Specialty
Unknown
Advisory Committee
Orthopedic
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
June 18, 2025
Date Received
May 20, 2025
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

to share the existing Gel-One manufacturing equipment in Preparation Building-3 in the SKK Takahagi Plant for the manufacture of another product, FHA-Gel-One

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MOZ Acid, Hyaluronic, Intraarticular