Identity
- Trade Name
- Stainless Steel Pan FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Model / Reference
- PAN FDA UDI
Identifiers
- Catalog Number
- PAN FDA UDI
- Primary DI / UDI-DI
- 10841307125891 FDA UDI
- 510(k) Number
- K200858 FDA UDI
- FDA Product Code
- KCT FDA UDI
- GMDN Term
- Device sterilization/disinfection container, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6850 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
Category: Device sterilization/disinfection container, reusable
Stainless Steel Pan by Implant Direct Sybron Manufacturing Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K200858 also covers:
- Drill Stop Kit - Long — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Drill Stop Kit - Long Empty — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Drill Stop Kit - Short — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Drill Stop Kit - Short Empty — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- InterActive®Surgical Kit Mini — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- InterActive®Surgical Kit Mini Empty — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Standard Surgical Kit Mini — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Standard Surgical Kit Mini Empty — IMPLANT DIRECT SYBRON MANUFACTURING LLC
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 II | Pending data |
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Manufacturer
- Manufacturer
- Implant Direct Sybron Manufacturing Llc
Sources (1)
- FDA UDI cb8f5118-fbe1-471a-ab9f-b42c6fcce5b4 35 fields · synced May 29, 2026