Kinamed, Inc.
United StatesFDA applicant, unverified FDA FEI 2027148
Kinamed, Inc. is a medical device manufacturer, with 353 devices listed in FDA GUDID and FDA 510(k) (FDA Class II, I and III) and 1 FDA recall as of 13 Nov 2026.
- Devices
- 353
- Registrations
- FDA
- FDA recalls
- 1
Registry facts
- Registries
- FDA GUDID 320
- FDA 510(k) 33
- Device classes
- FDA Class II 188
- FDA Class I 164
- FDA Class III 1
- FDA recalls
- Identifiers
- FDA FEI 2027148
- DUNS 184896645
At a glance
Market reach
- United States
- FDA FEI, FDA recalls
What Kinamed, Inc. makes
Kinamed, Inc. manufactures orthopaedic surgical procedure kits, including both reusable and single-use options, alongside orthopaedic bone screws and non-sliding fixation hardware. Their product portfolio also includes craniofacial bone screws, cranioplasty plates and sheets, craniofacial fixation plates, and non-fixed medical gas cylinder regulators.
These products are listed in the FDA UDI database and have received FDA 510(k) clearance.
Catalogue
Search and filter all 353 devicesShowing 1-50 of 353
Company details
- FDA FEI number
- 2027148
- DUNS number
- 184896645
- Address
- 820 Flynn Rd, CAMARILLO, CA, 93012
FDA recalls
FDA recall records list 1 recall initiated by Kinamed, Inc., initiated on 2010-08-18. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2010
- 18 Aug 2010 Z-2588-2011 Unclassified (pre-2012) Terminated The recall was initiated due to inadequate mechanical strength of these screwdrivers' hexagonal tip feature, causing it to strip during final tightening.
Frequently asked questions
How many devices does Kinamed, Inc. have in the registry?
The registry currently lists 353 devices for Kinamed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kinamed, Inc.'s devices?
Among its 50 most recently registered devices, Kinamed, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Kinamed, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Kinamed, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Kinamed, Inc.?
FDA recall records list 1 recall initiated by Kinamed, Inc., the most recent initiated on 18 Aug 2010. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Kinamed, Inc. in the registry?
The most recently registered devices listed for Kinamed, Inc. include SuperCable® ISO-Elastic™ Cerclage System 35-800-3022, SuperCable® ISO-Elastic™ Cerclage System 35-800-3032, SuperCable® ISO-Elastic™ Cerclage System 35-800-3052 and SuperCable® ISO-Elastic™ Cerclage System 35-800-3122.