Mx 06-20

FDA UDI

Class I (US FDA UDI)

by Meta Biomed, Inc.

Identity

Trade Name: MX 06-20 FDA UDI
Generic Name: Synthetic gutta-percha FDA UDI
Device Name: MGP, 06 Taper 20, 60 Points, P.71 FDA UDI
Model / Reference: 1473 FDA UDI
Description: MGP, 06 Taper 20, 60 Points, P.71 FDA UDI

Identifiers

Primary DI / UDI-DI: 08806387814733 FDA UDI
FDA Product Code: EKM FDA UDI
GMDN Term: Synthetic gutta-percha FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3850 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Synthetic gutta-percha

Mx 06-20 by Meta Biomed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic gutta-percha.

Gutta Percha Points — ROYDENT DENTAL PRODUCTS INC · Class I
Roydent Gutta Percha — ROYDENT DENTAL PRODUCTS INC · Class I
Vortex Blue Conform Fit — TULSA DENTAL PRODUCTS LLC · Class I
Safco gutta percha points — Safco Dental Supply · Class I
Vortex Blue Conform Fit — TULSA DENTAL PRODUCTS LLC · Class I
EdgeSequel™ — US Endodontics, LLC · Class I
Gutta Percha Points — TULSA DENTAL PRODUCTS LLC · Class I
Henry Schein — HENRY SCHEIN, INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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

Manufacturer

Manufacturer: Meta Biomed, Inc.

Sources (1)

FDA UDI 229bc048-23f8-4d73-b347-11030053ce04 33 fields · synced May 31, 2026