Teligen 286202205S

by Medos International Sàrl

Teligen 286202205S is a Class II device made by Medos International Sàrl, cleared under FDA 510(k) K233254 on 14 Jun 2024 (2 earlier submissions) and listed in FDA GUDID since 10 Feb 2024 (UDI-DI 10705034604558), 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

+2 more

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK233254	Date14 Jun 2024Decided	StatusActive
United States	GUDID listing	Number10705034604558 UDI-DI	Date10 Feb 2024Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK223438	Date10 Feb 2023Decided	StatusActive
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK223108	Date19 Jan 2023Decided	StatusActive

Official records

AccessGUDID record UDI-DI 10705034604558
FDA 510(k) database 510(k) number K233254
FDA 510(k) database 510(k) number K223438
FDA 510(k) database 510(k) number K223108

Across registries

2 registries list this device

FDA 510(k) K233254 decided 14 Jun 2024 Active· +2 more in the status table
FDA GUDID UDI-DI 10705034604558 listed 10 Feb 2024 Listed

Timeline

4 dated events

19 Jan 2023 Cleared FDA 510(k) K223108
10 Feb 2023 Cleared FDA 510(k) K223438
10 Feb 2024 Listed FDA GUDID 10705034604558
14 Jun 2024 Cleared FDA 510(k) K233254

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Teligen
Generic name: Nerve-locating system probe, single-use
Model / reference: 286202205S

Primary DI / UDI-DI: 10705034604558
510(k) Number: K223108
K223438
K233254
FDA product code: PDQ, OLO
GMDN term: Nerve-locating system probe, single-use

Device class: Class II
Regulation number: 874.1820, 882.4560
GUDID distribution status: In Commercial Distribution

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Properties

Supplied sterile
Single use
Prescription use
Lot / batch number
Expiration date

Other properties (10, all answered No)