Identity
- Trade Name
- PRE-MADE ENG. XA POST FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- PRE-MADE ENG. XA POST H 1 MM D.3.30 MM FDA UDI
- Model / Reference
- SH-MD-F-330-1 FDA UDI
- Description
- PRE-MADE ENG. XA POST H 1 MM D.3.30 MM FDA UDI
Identifiers
- Catalog Number
- SH-MD-F-330-1 FDA UDI
- Primary DI / UDI-DI
- D7701248413 FDA UDI
- 510(k) Number
- K162004 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
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dental implant suprastructure, permanent, preformed
Pre-Made Eng. Xa Post by Sweden & Martina Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental implant suprastructure, permanent, preformed.
- HS/HG Prosthetic System — OSSTEM IMPLANT Co., Ltd. · Class II
- DESS dental smart solutions — TERRATS MEDICAL SL. · Class II
- Diamodent — Diamodent · Class II
- Cemented Abutment — POINTIMPLANT Co., Ltd. · Class II
- GS System — OSSTEM IMPLANT Co., Ltd. · Class II
- Temporary Abutment — Cybermed Inc. · Class II
- EZ Post — Megagen Implant Co. Ltd · Class II
- Neodent — JJGC Indústria e Comércio de Materiais Dentários S/A. · Class II
Cleared under the same submission
K162004 also covers:
- ABUTMENT SCREW — SWEDEN & MARTINA INC
- ABUTMENT SCREW M1.8 — SWEDEN & MARTINA INC
- ABUTMENT SCREW M1.8 — SWEDEN & MARTINA INC
- ABUTMENT SCREW M1.8 — SWEDEN & MARTINA INC
- ABUTMENT SCREW M1.8 — SWEDEN & MARTINA INC
- ABUTMENT SCREW M1.8 — SWEDEN & MARTINA INC
- ANALOGUE FOR PRE-MADE — SWEDEN & MARTINA INC
- ANALOGUE FOR PRE-MADE — SWEDEN & MARTINA INC
- ANALOGUE FOR PRE-MADE — SWEDEN & MARTINA INC
- ANALOGUE FOR XA ABUTMENT — SWEDEN & MARTINA INC
- HEALING PEEK CAP. NARROW PROF. — SWEDEN & MARTINA INC
- PRE-MADE ENG. XA POST — SWEDEN & MARTINA 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 II | Pending data |
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Manufacturer
- Manufacturer
- Sweden & Martina Inc
Sources (1)
- FDA UDI 237b861f-ac13-4497-b7f1-8fa8705f16e3 36 fields · synced May 31, 2026