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PeriAcryl®

FDA UDI

Class II (US FDA UDI)

by Glustich Inc

Identity

Trade Name
PeriAcryl® FDA UDI
Generic Name
Clinical periodontal dressing FDA UDI
Device Name
PeriAcryl® is indicated to be used as an adjunct to temporarily assist in securing periodontal dressings. FDA UDI
Model / Reference
P-ACRYLU(C) FDA UDI
Description
PeriAcryl® is indicated to be used as an adjunct to temporarily assist in securing periodontal dressings. FDA UDI

Identifiers

Catalog Number
P-ACRYLU(C) FDA UDI
Primary DI / UDI-DI
D795020 FDA UDI
510(k) Number
K071484 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Clinical periodontal dressing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Clinical periodontal dressing

PeriAcryl® by Glustich Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Clinical periodontal dressing.

Cleared under the same submission

K071484 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Glustich Inc

Sources (1)

  • FDA UDI 8baea60e-5652-4a01-83f4-b0dffaf3cfd1 36 fields · synced Jun 1, 2026