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Bosworth

FDA UDI

Class I (US FDA UDI)

by Keystone Industries

Identity

Trade Name
Bosworth FDA UDI
Generic Name
Dental wedge, single-use FDA UDI
Device Name
WONDER WEDGES-12MM Small, Natural (100) FDA UDI
Model / Reference
0921417 FDA UDI
Description
WONDER WEDGES-12MM Small, Natural (100) FDA UDI

Identifiers

Catalog Number
0921417 FDA UDI
Primary DI / UDI-DI
H66809214171 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Dental wedge, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 12 Millimeter FDA UDI

Category: Dental wedge, single-use

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

Similar devices

Also classified as Dental wedge, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Keystone Industries

Sources (1)

  • FDA UDI e24b197f-9d8f-4dc7-86d9-2c931195a96d 36 fields · synced Jun 9, 2026