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Lowman Bone Holding Clamp

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Lowman Bone Holding Clamp FDA UDI
Generic Name
Bone approximation clamp FDA UDI
Device Name
Lowman Bone Holding Clamp 1 X 2 Prongs FDA UDI
Model / Reference
305-465 FDA UDI
Description
Lowman Bone Holding Clamp 1 X 2 Prongs FDA UDI

Identifiers

Primary DI / UDI-DI
00192896105713 FDA UDI
FDA Product Code
HXD FDA UDI
GMDN Term
Bone approximation clamp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 7.25 Inch FDA UDI

Category: Bone approximation clamp

Lowman Bone Holding Clamp by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone approximation clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 80f473c0-1ee7-42d7-924c-5c29e0b16e00 35 fields · synced May 31, 2026