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Spotlight

FDA UDI

Class II (US FDA UDI)

by Depuy Spine, Inc.

Identity

Trade Name
SPOTLIGHT FDA UDI
Generic Name
Fibreoptic retractor handle FDA UDI
Device Name
SPOTLIGHT PL RETRACTOR HANDLE FDA UDI
Model / Reference
282950000 FDA UDI
Description
SPOTLIGHT PL RETRACTOR HANDLE FDA UDI

Identifiers

Catalog Number
282950000 FDA UDI
Primary DI / UDI-DI
10705034358994 FDA UDI
510(k) Number
K113273 FDA UDI
FDA Product Code
GZT FDA UDI
FSQ FDA UDI
GMDN Term
Fibreoptic retractor handle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 FDA UDI
878.4580 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: Fibreoptic retractor handle

Spotlight by Depuy Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic retractor handle.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy Spine, Inc.

Sources (1)

  • FDA UDI 5a777ac6-38f8-43bc-84bc-1623a2cfe710 36 fields · synced Jun 8, 2026