LEVEL ONE CMF

GUDID 00888118143389

PLATE, ORTHOG, BSSO, CVD, 4 MM BRG, 2.0 MM SCREW, TI-6AL-4V

KLS-Martin L.P.

Craniofacial fixation plate, non-bioabsorbable, non-customized

• Primary Device ID: 00888118143389
• NIH Device Record Key: b4f3613a-be0d-477b-8574-ca6ba9c90154
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LEVEL ONE CMF
• Version Model Number: 50-330-08-09
• Company DUNS: 826499238
• Company Name: KLS-Martin L.P.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com
• Phone: +1(904)641-7746
• Email: KLS-UDI-Info@klsmartin.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888118143389 [Primary]

FDA Product Code

• JEY: PLATE, BONE

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00888118143389]

Moist Heat or Steam Sterilization

[00888118143389]

Moist Heat or Steam Sterilization

[00888118143389]

Moist Heat or Steam Sterilization

[00888118143389]

Moist Heat or Steam Sterilization

[00888118143389]

Moist Heat or Steam Sterilization

[00888118143389]

Moist Heat or Steam Sterilization

[00888118143389]

Moist Heat or Steam Sterilization

[00888118143389]

Moist Heat or Steam Sterilization

[00888118143389]

Moist Heat or Steam Sterilization

[00888118143389]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-10-02
• Device Publish Date: 2025-09-24

On-Brand Devices [LEVEL ONE CMF]

• 10888118113921: SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V
• 10888118113914: SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V
• 10888118113907: SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V
• 10888118113891: SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V
• 10888118113884: SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V
• 10888118113877: SCREW, MAXDRIVE, TLTS, TAPERED, TI-6AL-4V
• 10888118113617: SCREW, ONEDRIVE, DRILL FREE, TI-6AL-4V
• 10888118113600: SCREW, ONEDRIVE, DRILL FREE, TI-6AL-4V
• 10888118113549: SCREW, MAXDRIVE, MMF, DRILL FREE, WIDE THD, 46* FLUTE, STAINLESS STEEL ASTM F138
• 10888118113532: SCREW, MAXDRIVE, MMF, DRILL FREE, WIDE THD, 46* FLUTE, STAINLESS STEEL ASTM F138
• 10888118102215: SCREW, MAXDRIVE, MMF, DRILL FREE, WIDE THD, STAINLESS STEEL ASTM F138
• 10888118102208: SCREW, MAXDRIVE, MMF, DRILL FREE, WIDE THD, STAINLESS STEEL ASTM F138
• 10888118095371: SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
• 10888118095364: SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
• 10888118095357: SCREW, MAXDRIVE, F3, TI-6AL-4V
• 10888118095340: SCREW, MAXDRIVE, F3, TI-6AL-4V
• 10888118095333: SCREW, MAXDRIVE, F3, EMERGENCY, TI-6AL-4V
• 10888118095326: SCREW, MAXDRIVE, F3, EMERGENCY, TI-6AL-4V
• 10888118095319: SCREW, MAXDRIVE, F3, TI-6AL-4V
• 10888118095302: SCREW, MAXDRIVE, F3, TI-6AL-4V
• 10888118095296: SCREW, MAXDRIVE, F3, TI-6AL-4V
• 10888118094619: SCREW, MAXDRIVE, F3, TI-6AL-4V
• 10888118094602: SCREW, MAXDRIVE, F3, EMERGENCY, TI-6AL-4V
• 10888118094589: SCREW, MAXDRIVE, F3, TI-6AL-4V
• 10888118094565: SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
• 10888118094558: SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
• 10888118094541: SCREW, MAXDRIVE, F3, TI-6AL-4V
• 10888118094534: SCREW, MAXDRIVE, F3, TI-6AL-4V
• 10888118094527: SCREW, MAXDRIVE, FLAT TIP, TI-6AL-4V
• 10888118094510: SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
• 10888118094503: SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
• 10888118094497: SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
• 10888118094480: SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
• 10888118094473: SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
• 10888118094466: SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
• 10888118094459: SCREW, CROSSDRIVE, TLTS, EMERGENCY, TI-6AL-4V
• 10888118073553: SCREW, CROSSDRIVE, TLTS, FASTENING, TEMPORARY CONDYLAR IMPLANT, TI-6AL-4V
• 10888118073492: SCREW, CROSSDRIVE, TLCK, FASTENING, TEMPORARY CONDYLAR IMPLANT, TI-6AL-4V
• 10888118048728: SCREW, MAXDRIVE, TLTS, EMERGENCY, TI-6AL-4V
• 10888118048704: SCREW, MAXDRIVE, TLTS, EMERGENCY, TI-6AL-4V
• 10888118048681: SCREW, MAXDRIVE, TLTS, EMERGENCY, TI-6AL-4V
• 10888118048667: SCREW, MAXDRIVE, TLTS, EMERGENCY, TI-6AL-4V
• 10888118048643: SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
• 10888118048629: SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
• 10888118048605: SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
• 10888118048582: SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
• 10888118048568: SCREW, MAXDRIVE, EMERGENCY, TI-6AL-4V
• 10888118048544: SCREW, MAXDRIVE, TLTS, TI-6AL-4V
• 10888118048520: SCREW, MAXDRIVE, TLTS, TI-6AL-4V
• 10888118048506: SCREW, MAXDRIVE, TLTS, TI-6AL-4V