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One Stage TL Standard Plus

FDA UDI

Class II (US FDA UDI)

by I3 Implant Llc

Identity

Trade Name
One Stage TL Standard Plus FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Model / Reference
I3012080 FDA UDI

Identifiers

Primary DI / UDI-DI
00810027863348 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screw endosteal dental implant, two-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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Screw endosteal dental implant, two-piece

One Stage TL Standard Plus by I3 Implant Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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 11831a88-b782-4a54-82bf-5bc2da8db13b 32 fields · synced May 31, 2026