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Bone Level Implant

FDA UDI

Class II (US FDA UDI)

by I3 Implant Llc

Identity

Trade Name
Bone Level Implant FDA UDI
Generic Name
Dental implant system FDA UDI
Model / Reference
I3162010 FDA UDI

Identifiers

Primary DI / UDI-DI
00810027861733 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant system 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

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant system

Bone Level Implant by I3 Implant Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
I3 Implant Llc

Sources (1)

  • FDA UDI 59fd7857-c825-4c12-9a4c-d8923048ac92 32 fields · synced Jun 1, 2026