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Level One Cmf 50-766-06-09

by KLS-Martin L.P.

Level One Cmf 50-766-06-09 is a Class II device made by KLS-Martin L.P., listed in FDA GUDID since 24 Mar 2016 (UDI-DI 00888118078322), 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 Number00888118078322 UDI-DI Date24 Mar 2016ListedStatusListed 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  • Withdrawn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
Level One Cmf
Generic name
Craniofacial fixation plate, non-bioabsorbable, non-customized
Model / reference
50-766-06-09
Primary DI / UDI-DI
00888118078322
FDA product code
MQN
GMDN term
Craniofacial fixation plate, non-bioabsorbable, non-customized
Device class
Class II
Regulation number
872.4760
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Conditional

Related devices

Category: Craniofacial fixation plate, non-bioabsorbable, non-customized

Other devices from KLS-Martin L.P.

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

Properties

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