Identity
- Trade Name
- Henry Schein FDA UDI
- Generic Name
- Dental power tool system handpiece, pneumatic FDA UDI
- Device Name
- Contra Angle Deluxe Sectional FDA UDI
- Model / Reference
- 1003003 FDA UDI
- Description
- Contra Angle Deluxe Sectional FDA UDI
Identifiers
- Catalog Number
- 1003003 FDA UDI
- Primary DI / UDI-DI
- 00304040057766 FDA UDI
- 510(k) Number
- K073652 FDA UDI
- FDA Product Code
- EFB FDA UDI
- GMDN Term
- Dental power tool system handpiece, pneumatic FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4200 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dental power tool system handpiece, pneumatic
Henry Schein by Henry Schein, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental power tool system handpiece, pneumatic.
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- PROPHY SPORT — HANDPIECE PARTS & REPAIRS, INC. · Class I
- MK-dent Germany® — MK-Dent GmbH · Class I
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- MK-dent Germany® — MK-Dent GmbH · Class I
Cleared under the same submission
K073652 also covers:
- Darby Dental Supply, LLC — DARBY DENTAL SUPPLY, LLC
- Darby Dental Supply, LLC — DARBY DENTAL SUPPLY, LLC
- Henry Schein — HENRY SCHEIN, INC.
- Henry Schein — HENRY SCHEIN, INC.
- Henry Schein — HENRY SCHEIN, INC.
- Henry Schein — HENRY SCHEIN, INC.
- Henry Schein — HENRY SCHEIN, INC.
- Henry Schein — HENRY SCHEIN, INC.
- Henry Schein — HENRY SCHEIN, INC.
- Henry Schein — HENRY SCHEIN, INC.
- Henry Schein — HENRY SCHEIN, INC.
- Henry Schein — HENRY SCHEIN, 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
- Henry Schein, Inc.
Sources (1)
- FDA UDI 15621f6d-6a21-4b33-9482-6ff1d1236ee3 35 fields · synced Jun 8, 2026