LOCON
GUDID 00840420133069
WRIGHT MEDICAL TECHNOLOGY, INC.
Orthopaedic bone screw, non-bioabsorbable, non-sterile| Primary Device ID | 00840420133069 |
| NIH Device Record Key | 655451e1-2696-4a02-92bf-2c852c1eb0bd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LOCON |
| Version Model Number | 49000218 |
| Company DUNS | 807201207 |
| Company Name | WRIGHT MEDICAL TECHNOLOGY, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com |
Device Dimensions
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 1.8 Millimeter |
| Length | 20 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840420133069 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K033456
FDA Product Code
| HRS | PLATE, FIXATION, BONE |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
[00840420133069]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-15 |
On-Brand Devices [LOCON]
| 00889797059534 | 79010010 |
| 00889797001151 | 24900036 |
| 00840420134851 | 24934726 |
| 00840420134844 | 24934724 |
| 00840420134837 | 24934722 |
| 00840420134820 | 24934720 |
| 00840420134813 | 24934718 |
| 00840420134806 | 24934716 |
| 00840420134790 | 24934714 |
| 00840420134783 | 24933726 |
| 00840420134776 | 24933724 |
| 00840420134769 | 24933722 |
| 00840420134752 | 24933720 |
| 00840420134745 | 24933718 |
| 00840420134738 | 24933716 |
| 00840420134721 | 24933714 |
| 00840420134714 | 24933712 |
| 00840420134417 | 7900LNGR |
| 00840420134400 | 7900LNGL |
| 00840420134394 | 7900STDR |
| 00840420134387 | 7900STDL |
| 00840420133397 | 49000740 |
| 00840420133380 | 49000738 |
| 00840420133373 | 49000736 |
| 00840420133342 | 49000730 |
| 00840420133120 | 49000230 |
| 00840420133083 | 49000222 |
| 00840420133069 | 49000218 |
| 00840420132987 | 49000MDR |
| 00840420132970 | 49000MDL |
| 00889797059527 | Drill Bit |
Trademark Results [LOCON]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LOCON 76604295 3093705 Dead/Cancelled |
Wright Medical Technology, Inc. 2004-07-26 |
 LOCON 73732184 1526620 Live/Registered |
LOCON SENSOR SYSTEMS, INC. 1988-06-02 |
 LOCON 73588715 not registered Dead/Abandoned |
SCHLUTER FOTOSENSORIK GMBH & CO. KG. 1986-03-18 |
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