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Multi Unit Sleave

FDA UDI

Class II (US FDA UDI)

by Dentack Implants Ltd

Identity

Trade Name
Multi Unit Sleave FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
Multi Unit Sleave FDA UDI
Model / Reference
MUA-230 FDA UDI
Description
Multi Unit Sleave FDA UDI

Identifiers

Primary DI / UDI-DI
07290112280206 FDA UDI
510(k) Number
K152188 FDA UDI
FDA Product Code
DZE FDA UDI
NHA 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
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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Dry Heat Sterilization FDA UDI

Category: Screw endosteal dental implant, two-piece

A comprehensive medical device directory listing the Multi Unit Sleave, a screw endosteal dental implant. It is designed to provide support and retention for a dental prosthesis (e.g., bridge, single-tooth, overdenture) in the mandible or maxilla.

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e6fbe684-8997-4cf2-924e-57604eb296aa 35 fields · synced Aug 3, 2026