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Reconstructive Wedge

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
Reconstructive Wedge FDA UDI
Generic Name
Laryngoscope handle, single-use FDA UDI
Model / Reference
110004033 FDA UDI

Identifiers

Catalog Number
110004033 FDA UDI
Primary DI / UDI-DI
00887868371202 FDA UDI
510(k) Number
K122770 FDA UDI
FDA Product Code
HRS FDA UDI
HWC FDA UDI
GMDN Term
Laryngoscope handle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
888.3040 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

Category: Laryngoscope handle, single-use

Reconstructive Wedge by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope handle, single-use.

Cleared under the same submission

K122770 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Orthopedics, Inc.

Sources (1)

  • FDA UDI 008b09a7-5308-4adf-85fc-f291b3f3cdd8 36 fields · synced Jun 1, 2026