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Permlastic

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Permlastic FDA UDI
Generic Name
Polysulfide dental impression material FDA UDI
Device Name
Impression material catalyst, regular bodied FDA UDI
Model / Reference
00494 FDA UDI
Description
Impression material catalyst, regular bodied FDA UDI

Identifiers

Primary DI / UDI-DI
00841396118647 FDA UDI
510(k) Number
K003650 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Polysulfide dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Dimensions & Sizes

Size
Weight — 130 Gram FDA UDI

Category: Polysulfide dental impression material

Permlastic by Kerr Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polysulfide dental impression material.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI ceb0708e-08fe-4f5e-901c-00326fff35ee 37 fields · synced Jun 8, 2026