Joints 6.11

by Medstrat, Inc.

Joints 6.11 is a Class II device made by Medstrat, Inc., cleared under FDA 510(k) K051745 on 14 Jul 2005 and listed in FDA GUDID since 9 Aug 2025 (UDI-DI 00817886020660), active as of 22 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 22 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00817886020660 UDI-DI	Date9 Aug 2025Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Abbreviated	NumberK051745	Date14 Jul 2005Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00817886020660
FDA 510(k) database 510(k) number K051745

Across registries

2 registries list this device

FDA 510(k) K051745 decided 14 Jul 2005 Active
FDA GUDID UDI-DI 00817886020660 listed 9 Aug 2025 Listed

Timeline

2 dated events

14 Jul 2005 Cleared FDA 510(k) K051745
9 Aug 2025 Listed FDA GUDID 00817886020660

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Joints
Generic name: Radiological PACS-dedicated management software
Model / reference: 6.11

Primary DI / UDI-DI: 00817886020660
510(k) Number: K051745
FDA product code: LLZ
GMDN term: Radiological PACS-dedicated management software

Device class: Class II
Regulation number: 892.2050
GUDID distribution status: In Commercial Distribution

Similar devices

Other devices filed under FDA product code LLZ (System, Image Processing, Radiological).

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Properties

Lot / batch number

Other properties (14, all answered No)