Relieva Vortex 2 RV02Z

by Acclarent, Inc.

Relieva Vortex 2 RV02Z is a Class I device made by Acclarent, Inc., listed in FDA GUDID since 1 Oct 2016 (UDI-DI 20705031205885), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number20705031205885 UDI-DI	Date1 Oct 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 20705031205885

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Relieva Vortex 2
Generic name: Paranasal sinus irrigation catheter
Model / Ref / Catalog: RV02Z

Primary DI / UDI-DI: 20705031205885
FDA product code: KAR
GMDN term: Paranasal sinus irrigation catheter

Device class: Class I
Regulation number: 874.4420
GUDID distribution status: In Commercial Distribution

Similar devices

Other devices filed under FDA product code KAR (IRRIGATOR, SINUS).

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Properties

Supplied sterile
Single use
Prescription use
Premarket exempt
Lot / batch number
Expiration date
Manufacturing date

Other properties (8, all answered No)