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FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower

Also registered as Flower Orthopedics Corporation DBA Conventus Flower Orthoped, Flower Orthopedics Corporation Dba Conventus Flower Ortho

Country not established FDA establishment FEI 3009996260

Devices
4
Registrations
FDA
FDA recalls
0

What FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower makes

FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower manufactures Flex-Thread™ Distal Fibula Intramedullary Nail System and Flex-Thread™ Ulna Intramedullary Nail System, which are orthopedic devices used for internal fixation of fractures.

These devices are Class II and listed in the FDA 510(k) registry. The company is based in the US.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

Company details

FDA FEI number
3009996260
Address
100 Witmer Rd Ste 280, Horsham, PA, 19044

Frequently asked questions

How many devices does FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower have in the registry?

The registry currently lists 4 devices for FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower. Devices recorded under merged duplicate company entries are counted once.

Which registries list FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower's devices?

Among its 4 most recently registered devices, FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower has devices listed in FDA 510(k) (4 devices).

What risk classes do FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower's devices fall under?

Among its 4 most recently registered devices, the classes recorded for FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower in the registry?

The most recently registered devices listed for FLOWER ORTHOPEDICS CORPORATION DBA Conventus Flower include OsteoCoil™ GT Active Compression System, OsteoCoil™ Nitinol Compression System (Multiple Component PNs), Flex-Thread™ Distal Fibula lntramedullary Nail System and Flex-Thread™ Ulna Intramedullary Nail System.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.