Identity
- Trade Name
- Periosteal Elevator 6mm Width FDA UDI
- Generic Name
- Bone curette, reusable FDA UDI
- Device Name
- Periosteal Elevator 6mm Width FDA UDI
- Model / Reference
- 110625 FDA UDI
- Description
- Periosteal Elevator 6mm Width FDA UDI
Identifiers
- Catalog Number
- 110625 FDA UDI
- Primary DI / UDI-DI
- 00816950028533 FDA UDI
- 510(k) Number
- K152000 FDA UDI
- FDA Product Code
- HTE FDA UDI
- GMDN Term
- Bone curette, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
- Width — 6 Millimeter FDA UDI
Category: Bone curette, reusable
Periosteal Elevator 6mm Width by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Bone curette, reusable.
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- Novo Surgical — NOVO SURGICAL, INC. · Class I
- Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
- Volkmann Bone Curette Oval - Fig. 00 17 cm - 6 3/4" Scoop Size 4.4 mm Stainless Steel — SURTEX INSTRUMENTS LTD · 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 |
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Manufacturer
- Manufacturer
- OsteoCentric Technologies, Inc
Sources (1)
- FDA UDI 3c75473c-191c-43af-a27a-00099c84f18a 37 fields · synced May 30, 2026