Identity
- Trade Name
- Large Depth Gauge 125mm FDA UDI
- Generic Name
- Surgical depth gauge, reusable FDA UDI
- Device Name
- Large Depth Gauge 125mm FDA UDI
- Model / Reference
- 110202 FDA UDI
- Description
- Large Depth Gauge 125mm FDA UDI
Identifiers
- Catalog Number
- 110202 FDA UDI
- Primary DI / UDI-DI
- 00816950029530 FDA UDI
- 510(k) Number
- K152000 FDA UDI
- FDA Product Code
- HTJ FDA UDI
- GMDN Term
- Surgical depth gauge, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4300 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Depth — 125 Millimeter FDA UDI
Category: Surgical depth gauge, reusable
Large Depth Gauge 125mm by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical depth gauge, reusable.
- Depth Gauge — I.T.S. GmbH · Class I
- FO NX Nail System — FIELD ORTHOPAEDICS PTY LTD · Class I
- FO Micro Screw System — FIELD ORTHOPAEDICS PTY LTD · Class I
- Summa Orthopaedics System Surgical Instrument — Jeil Medical Corporation · Class I
- Trigen — Smith & Nephew, Inc. · Class I
- HOOK TIP DEPTH GAUGE CLAVICLE SYSTEM — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class I
- MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
- Summa Orthopaedics System Surgical Instrument — Jeil Medical Corporation · Class I
Cleared under the same submission
K152000 also covers:
- 1.5Nm Torque Limiter, AO — OsteoCentric Technologies,Inc
- 2.0mm Drill Bit 100mm — OsteoCentric Technologies,Inc
- 2.0mm Drill Bit Calibrated 110mm — OsteoCentric Technologies,Inc
- 2.0mm Drill Calibrated 145mm — OsteoCentric Technologies,Inc
- 2.0mm Threaded Drill Guide Calibrated — OsteoCentric Technologies,Inc
- 2.5 Hex Driver Long — OsteoCentric Technologies,Inc
- 2.5mm Drill Bit 180mm — OsteoCentric Technologies,Inc
- 2.5mm Drill Bit Calibrated 200mm — OsteoCentric Technologies,Inc
- 2.5mm Hex Driver Fixed 300mm — OsteoCentric Technologies,Inc
- 2.5mm Hex Driver Fixed Silicon Handle — OsteoCentric Technologies,Inc
- 2.5mm Hex Driver Sleeve — OsteoCentric Technologies,Inc
- 2.5mm Hex Driver w/AO Adapter — OsteoCentric Technologies,Inc
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- OsteoCentric Technologies, Inc
Sources (1)
- FDA UDI 393af535-b841-4dd9-95bd-5ed313626292 37 fields · synced May 30, 2026