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Solstice Occipito-Cervico-Thoracic System

FDA UDI

Class II (US FDA UDI)

by Life Spine, Inc.

Identity

Trade Name
Solstice Occipito-Cervico-Thoracic System FDA UDI
Generic Name
Manual orthopaedic bender, reusable FDA UDI
Device Name
Solstice OCT Tube Style Bender FDA UDI
Model / Reference
117-992 FDA UDI
Description
Solstice OCT Tube Style Bender FDA UDI

Identifiers

Catalog Number
117-992 FDA UDI
Primary DI / UDI-DI
00190837040048 FDA UDI
510(k) Number
K090343 FDA UDI
FDA Product Code
KWP FDA UDI
GMDN Term
Manual orthopaedic bender, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3050 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: Manual orthopaedic bender, reusable

Solstice Occipito-Cervico-Thoracic System by Life Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual orthopaedic bender, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Life Spine, Inc.

Sources (1)

  • FDA UDI bc0914fe-2da7-47e1-afd5-4617e6ef4327 35 fields · synced Jun 8, 2026