Skip to content

Zavation Caddy 259-9000-C2

by Zavation

Zavation Caddy 259-9000-C2 is a Class II device made by Zavation, cleared under FDA 510(k) K180673 on 13 Jul 2018 and listed in FDA GUDID since 12 May 2026 (UDI-DI 00197157080839), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K180673

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00197157080839 UDI-DI Date12 May 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK180673 Date13 Jul 2018DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K180673 decided 13 Jul 2018 Active
  • FDA GUDID UDI-DI 00197157080839 listed 12 May 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K180673
  2. Listed FDA GUDID 00197157080839

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Zavation Caddy
Generic name
Instrument tray, reusable
Model / reference
259-9000-C2
Primary DI / UDI-DI
00197157080839
510(k) Number
FDA product code
PLR, MQP
GMDN term
Instrument tray, reusable
Device class
Class II
Regulation number
888.3060
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Cleared under the same submission (K180673)

and 8 more cleared under K180673

Other devices from Zavation

See all devices from Zavation →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)