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Ips 60-500-17-09-LP

by KLS-Martin L.P. 2 variants

Ips 60-500-17-09-LP is a Class II device made by KLS-Martin L.P., listed in FDA GUDID since 28 Sep 2026 (UDI-DI 00888118155535), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00888118155535 UDI-DI Date28 Sep 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Ips
Generic name
Fixed dental occlusal splint, custom-made
Model / reference
60-500-17-09-LP
Primary DI / UDI-DI
00888118155535
FDA product code
JEY, DZJ
GMDN term
Fixed dental occlusal splint, custom-made
Device class
Class II
Regulation number
872.4760, 872.4120
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Other devices from KLS-Martin L.P.

See all devices from KLS-Martin L.P. →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Serial number
Other properties (10, all answered No)