← Back to catalogue

Dispense-A-Tie Ligatures

FDA UDI

Class I (US FDA UDI)

by Tp Orthodontics, Inc.

Identity

Trade Name
Dispense-A-Tie Ligatures FDA UDI
Generic Name
Orthodontic archwire/bracket ligature FDA UDI
Device Name
Assorted FDA UDI
Model / Reference
383-013 FDA UDI
Description
Assorted FDA UDI

Identifiers

Primary DI / UDI-DI
00192029040287 FDA UDI
FDA Product Code
ECI FDA UDI
GMDN Term
Orthodontic archwire/bracket ligature FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic archwire/bracket ligature

Dispense-A-Tie Ligatures by Tp Orthodontics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic archwire/bracket ligature.

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 ddd3f83f-3152-4214-943a-043bffdd867e 33 fields · synced Jun 8, 2026