Exactech
GUDID B504OM31535000
Provision
Carpal tunnel release instrument Carpal tunnel release instrument Carpal tunnel release instrument Carpal tunnel release instrument Carpal tunnel release instrument Carpal tunnel release instrument Carpal tunnel release instrument Carpal tunnel release instrument Carpal tunnel release instrument Carpal tunnel release instrument Carpal tunnel release instrument Carpal tunnel release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument Hand ligament surgical release instrument| Primary Device ID | B504OM31535000 |
| NIH Device Record Key | 72fef257-8f2a-4c50-ae61-038f77be51f8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Exactech |
| Version Model Number | 315-35-00 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| 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 | true |
| 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
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B504OM31535000 [Primary] |
FDA Product Code
| LXH | Orthopedic Manual Surgical Instrument |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-09-29 |
| Device Publish Date | 2021-09-21 |
On-Brand Devices [Exactech]
| B504OM32115070 | 321-15-07 |
| B504OM32115060 | 321-15-06 |
| B504OM31535000 | 315-35-00 |
| B504OM32152070 | 321-52-07 |
| B504OM30111050 | 301-11-05 |
| B504OM32152090 | 321-52-09 |
| B504OM30111060 | 301-11-06 |
| B504OM31901320 | 319-01-32 |
| B504OM20178560 | 201-78-56 |
| B504OM52178330 | 521-78-33 |
| B504OM52178320 | 521-78-32 |
| B504OM52178310 | 521-78-31 |
| B504OM35190010 | 351-90-01 |
Trademark Results [Exactech]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 EXACTECH 97543105 not registered Live/Pending |
Exactech, Inc. 2022-08-10 |
 EXACTECH 86168270 not registered Dead/Abandoned |
Tyco Fire & Security GMBH 2014-01-17 |
 EXACTECH 79175410 4990914 Live/Registered |
Tyco Fire & Security GmbH 2015-08-09 |
 EXACTECH 77792130 3877806 Live/Registered |
Exactech, Inc. 2009-07-29 |
 EXACTECH 77792119 3868433 Live/Registered |
Exactech, Inc. 2009-07-29 |
 EXACTECH 77350327 not registered Dead/Abandoned |
Abbott Laboratories 2007-12-12 |
 EXACTECH 75132151 2115548 Dead/Cancelled |
Medisense, Inc. 1996-07-10 |
 EXACTECH 73804174 1650672 Dead/Cancelled |
EXACTECH, INC. 1989-06-01 |
 EXACTECH 73713884 1509981 Dead/Cancelled |
BAXTER TRAVENOL LABORATORIES, INC. 1988-02-29 |
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