Identity
- Trade Name
- Swish™ Healing Collar FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Model / Reference
- 9065-15 FDA UDI
Identifiers
- Catalog Number
- 9065-15 FDA UDI
- Primary DI / UDI-DI
- 10841307116219 FDA UDI
- 510(k) Number
- K081396 FDA UDI
- FDA Product Code
- NHA FDA UDI
- GMDN Term
- Dental implant suprastructure, permanent, preformed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3630 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Swish™ Healing Collar by Implant Direct Sybron Manufacturing Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K081396 also covers:
- 5.0mmD RePlant Dense Bone Drill — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- 6.0mmD RePlant Dense Bone Drill — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Cortical Bone Drill for 4.2mmD Implant — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Cortical Bone Drill for 5.7mmD Implant — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- RePlant Soft Bone Step Drill — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- RePlant® Straight Abutment — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- RePlant® Straight Contoured Abutment — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Replant Soft Bone Step Drill — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Replant Soft Bone Step Drill — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Replant Soft Bone Step Drill — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Replant Soft Bone Step Drill Short — IMPLANT DIRECT SYBRON MANUFACTURING LLC
- Step Drill (6-16mml) — 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 8bc83749-9ed6-44a2-bd46-be707ba863d2 37 fields · synced May 31, 2026