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Relieva Circa EP01

by Acclarent, Inc.

Relieva Circa EP01 is a Class I device made by Acclarent, Inc., listed in FDA GUDID since 1 Oct 2016 (UDI-DI 10705031230989), 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 Number10705031230989 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  • Withdrawn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 Circa
Generic name
Bone-coring punch, single-use
Model / Ref / Catalog
EP01
Primary DI / UDI-DI
10705031230989
FDA product code
KAX
GMDN term
Bone-coring punch, single-use
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone-coring punch, single-use

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)