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Keystone Industries

FDA UDI

Class I (US FDA UDI)

by Keystone Industries

Identity

Trade Name
Keystone Industries FDA UDI
Generic Name
Denture clasp, metal, preformed FDA UDI
Device Name
2L Pre-Formed Clasp Pkg 100 FDA UDI
Model / Reference
1271220 FDA UDI
Description
2L Pre-Formed Clasp Pkg 100 FDA UDI

Identifiers

Catalog Number
1271220 FDA UDI
Primary DI / UDI-DI
H66812712201 FDA UDI
FDA Product Code
EHP FDA UDI
GMDN Term
Denture clasp, metal, preformed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3285 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Denture clasp, metal, preformed

Keystone Industries by Keystone Industries — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture clasp, metal, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Keystone Industries

Sources (1)

  • FDA UDI f7f268f9-f4cb-439b-b2ca-1364f034efc7 35 fields · synced Jun 9, 2026