← Back to catalogue

Cobb Spinal Elevator

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
COBB SPINAL ELEVATOR FDA UDI
Generic Name
Bone lever/elevator, reusable FDA UDI
Device Name
COBB SPINAL ELEVATOR SMALL SHARP COBB TIP UNIQUE BLACK HANDLE FDA UDI
Model / Reference
320-627B FDA UDI
Description
COBB SPINAL ELEVATOR SMALL SHARP COBB TIP UNIQUE BLACK HANDLE FDA UDI

Identifiers

Catalog Number
320-627B FDA UDI
Primary DI / UDI-DI
00192896028296 FDA UDI
FDA Product Code
HTE FDA UDI
GMDN Term
Bone lever/elevator, reusable 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 — 17 Inch FDA UDI

Category: Bone lever/elevator, reusable

Cobb Spinal Elevator by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone lever/elevator, reusable.

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 2586900c-aeb9-4c79-9d30-df1e0d6f5c83 36 fields · synced Jun 8, 2026