Skip to content

Aria Free™ R0002

by Inova Labs, Inc. GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860003034712 UDI-DIDate27 Oct 2020ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Aria Free™
Generic Name
Sequential venous compression system
Model / Ref / Catalog
R0002
Primary DI / UDI-DI
00860003034712
510(k) Number
FDA Product Code
JOW
GMDN Term
Sequential venous compression system
Device Class
Class II
Regulation Number
870.5800
GUDID distribution status
Not in Commercial Distribution

Other devices from Inova Labs, Inc.

Properties

  • Prescription Use
  • Lot / Batch Number
  • Serial Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Expiration Date: No
  • Manufacturing Date: No