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Taperloc Complete

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
TAPERLOC COMPLETE FDA UDI
Generic Name
Bone file/rasp, manual, reusable FDA UDI
Model / Reference
51-206180 FDA UDI

Identifiers

Catalog Number
51-206180 FDA UDI
Primary DI / UDI-DI
00880304520776 FDA UDI
510(k) Number
K110400 FDA UDI
K120030 FDA UDI
FDA Product Code
LPH FDA UDI
JDI FDA UDI
MEH FDA UDI
OQG FDA UDI
KWZ FDA UDI
KWL FDA UDI
KWY FDA UDI
LZO FDA UDI
GMDN Term
Bone file/rasp, manual, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3350 FDA UDI
888.3353 FDA UDI
888.3310 FDA UDI
888.3360 FDA UDI
888.3390 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: Bone file/rasp, manual, reusable

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

Similar devices

Also classified as Bone file/rasp, manual, reusable.

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 116cde70-67eb-41e5-ab7d-c0f083689be5 36 fields · synced May 31, 2026