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Relieva Flex GC000RF

by Acclarent, Inc.

Relieva Flex GC000RF is a Class I device made by Acclarent, Inc., listed in FDA GUDID since 1 Oct 2016 (UDI-DI 10705031063372), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10705031063372 UDI-DI Date1 Oct 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Relieva Flex
Generic name
Paranasal sinus guide-catheter
Model / Ref / Catalog
GC000RF
Primary DI / UDI-DI
10705031063372
FDA product code
KAM
GMDN term
Paranasal sinus guide-catheter
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Paranasal sinus guide-catheter

Other devices from Acclarent, Inc.

See all devices from Acclarent, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)