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Montgomery® Thyroplasty Instrument

FDA UDI

Class II (US FDA UDI)

by Boston Medical Products, Inc.

Identity

Trade Name
Montgomery® Thyroplasty Instrument FDA UDI
Generic Name
ENT elevator FDA UDI
Device Name
Chisel Elevator FDA UDI
Model / Reference
MT-211 FDA UDI
Description
Chisel Elevator FDA UDI

Identifiers

Catalog Number
MT-211 FDA UDI
Primary DI / UDI-DI
EBESMT2110 FDA UDI
510(k) Number
K972317 FDA UDI
FDA Product Code
MIX FDA UDI
GMDN Term
ENT elevator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3620 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: ENT elevator

Montgomery® Thyroplasty Instrument by Boston Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT elevator.

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 46874d0b-4c68-4211-9e45-b83055acb7da 37 fields · synced Jun 9, 2026