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Swish™ Angled Contoured PS Abutment

FDA UDI

by Implant Direct Sybron Manufacturing Llc

Identity

Trade Name
Swish™ Angled Contoured PS Abutment FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Model / Reference
9065-52P FDA UDI

Identifiers

Catalog Number
9065-52P FDA UDI
Primary DI / UDI-DI
10841307115601 FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Commercial Distribution
Not 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

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Swish™ Angled Contoured PS Abutment by Implant Direct Sybron Manufacturing Llc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b17050ba-ccd5-474c-ad8a-ce4d019a26c1 36 fields · synced Jun 8, 2026