Surgical Direct

Surgical Headlight..1 - Headgear light weight single back adjustment..1 - Black headlight module, 90° 10-100mm variable spot..2 - Joysticks, detachable..1 - Set of cushioned detachable Blue…

Registry build 21.09.26

Surgical Headlight..1 – Headgear light weight single back adjustment..1 – Black headlight module, 90° 10-100mm variable spot..2 – Joysticks, detachable..1 – Set of cushioned detachable Blue foam sweatbands..1 – Mono-cable, 9ft with Wolf lens proximal

1manufacturer
4catalogue numbers in this listing

Who Else Makes It

Registered in Shandong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code FST
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42

Record

Regulatory record for Surgical Direct
Listed by Surgical Direct, Inc., United States
FDA product code FST
Device type Light, Surgical, Fiberoptic
Device class Class 2
Regulation 21 CFR 878.4580
Establishment Repacker / relabeller
510(k) K061690
Record published 2020-04-28
Record revised 2024-04-17 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number
Sizes Length 10100 cm

Catalogue Numbers

Catalogue numbers for Surgical Direct
Catalogue number Size Status
SD3100 Length 10100 cm In distribution
SD3120H Length 10100 cm In distribution
SD3115H Length 10100 cm In distribution
SD3200 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
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Fiberoptic Cable Black & Black Surgical, Inc. 17
MaXcess Nuvasive, Inc. 17
Integra® Integra Lifesciences (Ireland) Limited 16
Integra® Integra LifeSciences Production Corporation 14
Snowden-Pencer Steris Corporation 11
Vistor PRO LED Medical Illumination International, Inc 10

Showing 12 of 85. All products under Light, Surgical, Fiberoptic

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Surgical Direct
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Gulf Fiberoptics, Inc. 510(k) number 2011-05-13 Not classified Process control Gulf Medical Fiberoptics, Inc. recalled their Surgical Headlight because the cleaning instructions for the exterior surfaces of the headlight , headgear and fiber cable with 70% isopropyl alcohol had not been validated. 381 units 2012-08-28

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer