← Back to catalogue

LP Low Profile

FDA UDI

Class I (US FDA UDI)

by American Orthodontics

Identity

Trade Name
LP Low Profile FDA UDI
Generic Name
Orthodontic bracket, metal FDA UDI
Device Name
DB BRACKET LP MAX BICUSPID 197 PAD 5.5MM LANG 018 TQ=-6 A=0 R=0 FDA UDI
Model / Reference
973-3007M FDA UDI
Description
DB BRACKET LP MAX BICUSPID 197 PAD 5.5MM LANG 018 TQ=-6 A=0 R=0 FDA UDI

Identifiers

Catalog Number
973-3007M FDA UDI
Primary DI / UDI-DI
00190746089374 FDA UDI
FDA Product Code
EJF FDA UDI
GMDN Term
Orthodontic bracket, metal FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

LP Low Profile by American Orthodontics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 8b067b5c-5689-4c2a-86dd-5d95c1e8477d 36 fields · synced Jun 9, 2026