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LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 7.5 x 40

FDA UDI

Class II (US FDA UDI)

by Icotec

Identity

Trade Name
LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 7.5 x 40 FDA UDI
Generic Name
Spinal bone screw, non-bioabsorbable FDA UDI
Device Name
LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 7.5 x 40 mm FDA UDI
Model / Reference
16-6024-57540 FDA UDI
Description
LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 7.5 x 40 mm FDA UDI

Identifiers

Catalog Number
16-6024-57540 FDA UDI
Primary DI / UDI-DI
07640164849485 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Spinal bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Spinal bone screw, non-bioabsorbable

LightMore Pedicle System 6.0, Screw, Carbon/PEEK, Polyax., Noncann., Ø 7.5 x 40 by Icotec — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Spinal bone screw, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Icotec

Sources (1)

  • FDA UDI 06e6661c-64ab-4046-a96c-17e360a2c0ba 35 fields · synced Jun 8, 2026