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1788 1788210105

by Stryker Corp.

1788 1788210105 is a Class II device made by Stryker Corp., cleared under FDA 510(k) K230605 on 31 Mar 2023 and listed in FDA GUDID since 18 Apr 2023 (UDI-DI 07613327580037), 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) K230605

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 Number07613327580037 UDI-DI Date18 Apr 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK230605 Date31 Mar 2023DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K230605 decided 31 Mar 2023 Active
  • FDA GUDID UDI-DI 07613327580037 listed 18 Apr 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K230605
  2. Listed FDA GUDID 07613327580037

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
1788
Generic name
Endoscope video camera
Model / Ref / Catalog
1788210105
Primary DI / UDI-DI
07613327580037
510(k) Number
FDA product code
GCJ
GMDN term
Endoscope video camera
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Hydrogen Peroxide

Related devices

Category: Endoscope video camera

Cleared under the same submission (K230605)

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Sterilise before use
  • Serial number
Other properties (13, all answered No)