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Knit-Pak+

FDA UDI

Class U (US FDA UDI)

by Premier Dental Products Company

Identity

Trade Name
Knit-Pak+ FDA UDI
Generic Name
Gingival retraction cord, non-medicated FDA UDI
Device Name
Premier® Knit-Pak™+ Aluminum Chloride Impregnated Retraction Cord, Dark Green - Size 000.0, Length – 100inch(254cm) FDA UDI
Model / Reference
9007560 FDA UDI
Description
Premier® Knit-Pak™+ Aluminum Chloride Impregnated Retraction Cord, Dark Green - Size 000.0, Length – 100inch(254cm) FDA UDI

Identifiers

Primary DI / UDI-DI
00348783001792 FDA UDI
510(k) Number
K132526 FDA UDI
FDA Product Code
MVL FDA UDI
GMDN Term
Gingival retraction cord, non-medicated FDA UDI

Classification

Device Class
U 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

Yes

FDA UDI

Category: Gingival retraction cord, non-medicated

Knit-Pak+ by Premier Dental Products Company — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction cord, non-medicated.

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 f60f0b2a-0947-445c-84c4-0fed4266a44a 34 fields · synced May 30, 2026