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Na 213-63-23

by Exactech, Inc. GUDID

Listed (no authorization) FDA GUDID database listing only

Regulatory status

as of 27 Oct 2026

Recall ongoing. 5 ongoing FDA recalls. See recalls

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885862059802 UDI-DIDate25 Aug 2022ListedStatusIn distribution

Coverage

1 jurisdiction

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

United States — GUDID listing Listed

Recalls

7 recalls · 5 ongoing · FDA

  • 4 recalls, same reason

    • Ongoing Z-2157-2024 FDA Class II initiated 18 Apr 2024
    • Ongoing Z-2156-2024 FDA Class II initiated 18 Apr 2024
    • Ongoing Z-2155-2024 FDA Class II initiated 18 Apr 2024
    • Ongoing Z-2158-2024 FDA Class II initiated 18 Apr 2024

    Exactech is recalling all affected UHMWPE (ultra-high molecular weight polyethylene) knee patella components packaged in out of specification vacuum bags.

    • Ongoing Z-0582-2024 FDA Class II initiated 21 Nov 2023

    Exactech has received 3 complaints for 4 devices related to a loss of vacuum in the inner-most vacuum bag.

    • Terminated Z-2070-2012 FDA Class II initiated 23 Sep 2011

    Exactech, Inc. Gainesville, FL is recalling their Optetrak Cemented Trapezoid Tibial Tray, Size 1F/1T, 2F/1T and the Optetrak Rotating Bearing Knee Tibial Tray, Finned, Cemented Tibial Tray, Size 2F/1T. Both trays have the potential to be mislabeled.

    • Terminated Z-0347-05 FDA Unclassified (pre-2012) initiated 11 Nov 2004

    Implant was identified incorrectly at the time of manufacture and was then labeled and distributed with the incorrect size information.

Specification

GUDID

Trade Name
Na
Generic Name
Bone-resection orthopaedic reamer, reusable
Model / Ref / Catalog
213-63-23
Primary DI / UDI-DI
10885862059802
510(k) Number
FDA Product Code
JWH
GMDN Term
Bone-resection orthopaedic reamer, reusable
Device Class
Class II
Regulation Number
888.3560
Commercial Distribution
In Commercial Distribution
Size
Width — 23 Millimeter

Related devices

Category: Bone-resection orthopaedic reamer, reusable

Cleared under the same submission (K933610)

Show all (12)

Other devices from Exactech, Inc.

See all devices from Exactech, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Serial Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Manufacturing Date: No