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Zuga

FDA UDI

Class II (US FDA UDI)

by Zuga Medical, Inc.

Identity

Trade Name
Zuga FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Titanium Abutment, 5.0mm, 7.0mm height x 4.5mm gum height FDA UDI
Model / Reference
TAA-500-470 FDA UDI
Description
Titanium Abutment, 5.0mm, 7.0mm height x 4.5mm gum height FDA UDI

Identifiers

Primary DI / UDI-DI
00853768007619 FDA UDI
510(k) Number
K122664 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

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 suprastructure, permanent, preformed

Zuga by Zuga Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zuga Medical, Inc.

Sources (1)

  • FDA UDI 86e8de1a-8efa-4342-8164-bc37f4d81af3 35 fields · synced May 31, 2026