Lattus

Cephalad/Caudal 150mm Blade, AL

Registry build 21.09.26
34manufacturers in China registered for this device type
63catalogue numbers in this listing
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (7), Zhejiang (6). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GAD
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
B.Braun Medical (Suzhou) Co,.Ltd Suzhou Jiangsu Contract manufacturer 37
Suzhou Microport Orthorecon Co., Ltd. Suzhou Jiangsu Contract manufacturer 31
Xinhua Healthcare Industry Co., Limited Zibo Shandong Contract manufacturer 30
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Shanghai KiNETIC Medical Co Ltd Shanghai Shanghai Contract manufacturer 19
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235
Xinhua Surgical Instrument Co., Ltd. Zibo Shandong Manufacturer 222
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74

Showing 12 of 34. All 34 manufacturers in China registered for Retractor

Record

Regulatory record for Lattus
Listed by Seaspine Orthopedics Corporation, United States
FDA product code GAD
Device type Retractor
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2022-08-25
Record revised 2025-10-24 (version 3)

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

Catalogue Numbers

Catalogue numbers for Lattus
Catalogue number Size Status
LS-3510-100 In distribution
LS-1000-140 In distribution
LS-3510-180 In distribution
LT2-103250 In distribution
LS-3510-140 In distribution
LT2-002140 In distribution
LT2-002180 In distribution
LS-3511-150 In distribution
LS-1000-110 In distribution
LS-1000-160 In distribution
LS-3510-170 In distribution
LS-3511-120 In distribution
AS-0907 In distribution
LT2-002110 In distribution
LS-3510-130 In distribution
LS-3510-120 In distribution
LS-2000-150 In distribution
LS-1000-170 In distribution
LS-2000-100 In distribution
AS-0904 In distribution
LT2-002130 In distribution
LS-2000-130 In distribution
LS-2000-140 In distribution
LS-2000-170 In distribution
LS-2000-180 In distribution
LT2-003200 In distribution
AS-0905 In distribution
LS-3511-180 In distribution
LS-3511-160 In distribution
LT2-002090 In distribution
LT2-001700 In distribution
AS-0906 In distribution
LS-1000-130 In distribution
LS-3510-090 In distribution
LS-3510-110 In distribution
LS-1000-180 In distribution
LS-3510-150 In distribution
LT2-001500 In distribution
LS-3511-140 In distribution
LS-1000-150 In distribution
LS-3511-110 In distribution
LT2-103200 In distribution
LT2-002170 In distribution
LS-2000-160 In distribution
LT2-002160 In distribution
LT2-002100 In distribution
LT2-002150 In distribution
LT2-002120 In distribution
LS-3511-130 In distribution
LS-1000-120 In distribution
LS-1000-100 In distribution
LS-1000-090 In distribution
LS-2000-090 In distribution
LT2-001400 In distribution
LT2-103150 In distribution
LT2-003150 In distribution
LS-2000-120 In distribution
LS-2000-110 In distribution
LS-3511-100 In distribution
LS-3511-090 In distribution
LS-3511-170 In distribution
LT2-001600 In distribution
LS-3510-160 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Thompson Thompson Surgical Instruments, Inc. 4,354
Millennium Avalign Technologies, Inc. 2,128
Surtex Surtex Instruments Ltd 1,318
Life Instruments Life Instrument Corp. 1,135
Innomed, Inc. Innomed, Inc. 1,017
Aesculap Aesculap AG 1,013
RZ Medizintechnik GmbH RZ Medizintechnik Gmbh 973
Elmed Elmed, Inc. 919
Medtronic Reusable Instruments Medtronic Sofamor Danek, Inc. 891
Boss Instruments Boss Instruments, Ltd. 799
gSource Gsource, LLC. 753
Sklar® Sklar Corporation 753

Showing 12 of 2,238. All products under Retractor

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2024-05-17 Class II Under Investigation by firm Cranial Caudal Blades manufactured incorrectly could result in fracture and/or damage to the bone structure 21 units
2024-05-17 Class II Under Investigation by firm Cranial Caudal Blades manufactured incorrectly could result in fracture and/or damage to the bone structure 31 units

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