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G&H Reverse Pull Face Mask, Screws

FDA UDI

Class II (US FDA UDI)

by G&H Wire Company, Inc.

Identity

Trade Name
G&H REVERSE PULL FACE MASK, SCREWS FDA UDI
Generic Name
Orthodontic extraoral headgear FDA UDI
Device Name
REPLACEMENT KEYS AND SCREWS FOR SMALL REVERSE PULL FACEMASK (RPFMSM) FDA UDI
Model / Reference
RPFMRS FDA UDI
Description
REPLACEMENT KEYS AND SCREWS FOR SMALL REVERSE PULL FACEMASK (RPFMSM) FDA UDI

Identifiers

Primary DI / UDI-DI
10190886000403 FDA UDI
510(k) Number
K111169 FDA UDI
FDA Product Code
DZB FDA UDI
GMDN Term
Orthodontic extraoral headgear FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5500 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic extraoral headgear

G&H Reverse Pull Face Mask, Screws by G&H Wire Company, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic extraoral headgear.

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 500fba47-634f-4fb2-a38b-db7762f353cb 35 fields · synced Jun 8, 2026