Mp-2456

by Fujifilm Corporation

Mp-2456 is a Class II device made by Fujifilm Corporation, cleared under FDA 510(k) K122537 on 12 Apr 2013 (5 earlier submissions) and listed in FDA GUDID since 17 Jul 2021 (UDI-DI 04573596210345), 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

+5 more

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	Number04573596210345 UDI-DI	Date17 Jul 2021Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK122537	Date12 Apr 2013Decided	StatusActive
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK122341	Date26 Sep 2012Decided	StatusActive
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK111227	Date13 May 2011Decided	StatusActive
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK093488	Date20 Nov 2009Decided	StatusActive
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK080176	Date29 Feb 2008Decided	StatusActive
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK043196	Date30 Nov 2004Decided	StatusActive

Official records

AccessGUDID record UDI-DI 04573596210345
FDA 510(k) database 510(k) number K122537
FDA 510(k) database 510(k) number K122341
FDA 510(k) database 510(k) number K111227
FDA 510(k) database 510(k) number K093488
FDA 510(k) database 510(k) number K080176
FDA 510(k) database 510(k) number K043196

Across registries

2 registries list this device

FDA 510(k) K122537 decided 12 Apr 2013 Active· +5 more in the status table
FDA GUDID UDI-DI 04573596210345 listed 17 Jul 2021 Listed

Timeline

7 dated events

30 Nov 2004 Cleared FDA 510(k) K043196
29 Feb 2008 Cleared FDA 510(k) K080176
20 Nov 2009 Cleared FDA 510(k) K093488
13 May 2011 Cleared FDA 510(k) K111227
26 Sep 2012 Cleared FDA 510(k) K122341
12 Apr 2013 Cleared FDA 510(k) K122537
17 Jul 2021 Listed FDA GUDID 04573596210345

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Generic name: Needle guide, reusable
Model / reference: MP-2456

Primary DI / UDI-DI: 04573596210345
FDA product code: IYO, IYN, ITX
GMDN term: Needle guide, reusable

Device class: Class II
Regulation number: 892.1560, 892.1550, 892.1570
GUDID distribution status: In Commercial Distribution

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Properties

Sterilise before use
Prescription use
Serial number
Manufacturing date

Other properties (11, all answered No)