Device
TITANEX ULTRA DEPTH GAUGE for K-wire dia 0.9 mm?/?1.1 mm, 150 mm
Manufacturer
VILEX LLC
VILEX LLC
Model: UZ-DPTH-0911
DI: 00841731147004
Status: New
MRI: Labeling does not contain MRI Safety Information
Single-use: No
Rx: Yes
OTC: No
First Published: 2026-05-15
Current Version: 2026-05-25
Description
TITANEX ULTRA DEPTH GAUGE for K-wire dia 0.9 mm?/?1.1 mm, 150 mm
Sterilization
Method Types - Sterilization Method:
Moist Heat or Steam Sterilization
Device Sterile:
No
Sterilization Prior To Use:
Yes
Regulatory & Distribution
Record Status:
Published
Version Number:
1
Record Key:
f1760d64-9d2f-4cc2-a24e-0357ba6153b7
Distribution Status:
In Commercial Distribution
DUNS Number:
117502293
Device Count:
1
DM Exempt:
No
Premarket Exempt:
No
HCT/P:
No
Kit:
No
Combination Product:
No
Lot/Batch Tracked:
Yes
Serial Number Tracked:
No
Manufacturing Date Tracked:
No
Expiration Date Tracked:
No
Donation ID Number Tracked:
No
Labeled Contains NRL:
No
Labeled No NRL:
No
Identifiers
Device ID:
00841731147004
Type:
Primary
Issuing Agency:
GS1
GMDN
Code: 32845
Name: Surgical depth gauge, reusable
Definition:
A surgical instrument designed to measure the depth of a recess, usually to measure the depth of holes being drilled in bone so that the surgeon can determine the length of the bone screw to be used. It may take two forms: 1) a device with a moveable (sliding) centrepiece (a prong), the tip of which is inserted into the recess to read from a scale; 2) a circular disc with a central hole which is clipped to a drill bit so that the device slides up as the drill bit is advanced. This is a reusable device intended to be sterilized prior to use.
FDA Product Codes
HTJ
GAUGE, DEPTH
Premarket Submissions
Submission Number:
K250304
Supplement Number:
000
Device Sizes
Device Size - Size Text:
N/A
Device Size - Size Type:
Device Size Text, specify
Environmental Conditions
Storage Handling - Storage Handling Type:
Special Storage Condition, Specify
Storage Handling - Storage Handling Special Condition Text:
N/A