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2.5mm x 10 Simpler Mini HA Implant

FDA UDI

Class II (US FDA UDI)

by Simpler Implant Solutions Inc

Identity

Trade Name
2.5mm x 10 Simpler Mini HA Implant FDA UDI
Generic Name
Screw endosteal dental implant, one-piece FDA UDI
Device Name
Simpler Mini Hydroxylapatit Coated Dental Implant FDA UDI
Model / Reference
SM 5002 FDA UDI
Description
Simpler Mini Hydroxylapatit Coated Dental Implant FDA UDI

Identifiers

Catalog Number
SM 5002 FDA UDI
Primary DI / UDI-DI
D780SM50020 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screw endosteal dental implant, one-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

Yes

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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Screw endosteal dental implant, one-piece

2.5mm x 10 Simpler Mini HA Implant by Simpler Implant Solutions Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Screw endosteal dental implant, one-piece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aaaeb6e3-61aa-4ab5-bbfd-b73d82d906bb 34 fields · synced Jun 1, 2026