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Saftey Release Modules Medium

FDA UDI

Class II (US FDA UDI)

by Ortho Specialties

Identity

Trade Name
Saftey Release Modules Medium FDA UDI
Generic Name
Orthodontic extraoral headgear FDA UDI
Device Name
Safety Release Modules For Intraoral And Extraoral Headgear-20 Ounce Medium FDA UDI
Model / Reference
600-558 FDA UDI
Description
Safety Release Modules For Intraoral And Extraoral Headgear-20 Ounce Medium FDA UDI

Identifiers

Catalog Number
600-558 FDA UDI
Primary DI / UDI-DI
00842452100668 FDA UDI
510(k) Number
K961754 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

No

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

Saftey Release Modules Medium by Ortho Specialties — 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

Manufacturer
Ortho Specialties

Sources (1)

  • FDA UDI 6f425c28-2d6c-4309-9d3a-91bf20c4d31d 36 fields · synced Jun 1, 2026