← Back to catalogue

Superfit

FDA UDI

Class II (US FDA UDI)

by Applied Dental, Inc.

Identity

Trade Name
SUPERFIT FDA UDI
Generic Name
Surgical/medical face mask, single-use FDA UDI
Device Name
SUPERFIT Disposable Procedural Face masks, Ear Loops. Level II FDA UDI
Model / Reference
FMK-50 FDA UDI
Description
SUPERFIT Disposable Procedural Face masks, Ear Loops. Level II FDA UDI

Identifiers

Primary DI / UDI-DI
00814639024975 FDA UDI
510(k) Number
K123115 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical face mask, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 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

No

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: Surgical/medical face mask, single-use

Superfit by Applied Dental, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/medical face mask, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 9e5d994f-4a84-461a-839e-8256bf03f54e 35 fields · synced May 30, 2026