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FLOWER ORTHOPEDICS CORPORATION

Last updated May 24, 2026

What FLOWER ORTHOPEDICS CORPORATION makes

Flower Orthopedics Corporation manufactures orthopaedic fixation hardware, including non-bioabsorbable bone screws (both cannulated and non-sliding), fixation plates for joints like the metatarsophalangeal (MTP) region, and orthodontic anchoring screws. Their portfolio also includes reusable surgical tools such as implant templates and depth limiters, as well as orthopaedic bone wires and headless compression screws for internal fixation. Devices are designed for procedures like fracture stabilization, joint reconstruction, and bone alignment, with variations in thread profiles and screw lengths to accommodate different anatomical needs.

The company’s products are regulated under FDA classification as Class I and Class II devices, with most listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for surgical use in orthopaedic applications and must comply with relevant U.S. regulatory requirements for medical device safety and performance. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Flower Orthopedics Corporation primarily manufacture?

Flower Orthopedics Corporation specializes in orthopaedic fixation devices, including non-bioabsorbable bone screws (such as cannulated and non-sliding varieties), fixation plates for joints like the metatarsophalangeal (MTP) region, and orthodontic anchoring screws. Their portfolio also includes reusable surgical tools like implant templates and depth limiters, as well as orthopaedic bone wires and headless compression screws. These devices are designed for fracture stabilization, joint reconstruction, and bone alignment procedures.

Where is Flower Orthopedics Corporation based?

Flower Orthopedics Corporation is headquartered in the United States. The company’s location ensures compliance with U.S. regulatory standards for medical devices, including those governing orthopaedic hardware.

Are Flower Orthopedics Corporation’s devices listed in any regulatory registries?

Yes, many of Flower Orthopedics Corporation’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability in the orthopaedic fixation market.

How are Flower Orthopedics Corporation’s devices classified under FDA regulations?

Flower Orthopedics Corporation’s devices fall under FDA classifications of Class I and Class II. Class I devices generally pose minimal risk and may require less regulatory oversight, while Class II devices—such as certain orthopaedic fixation hardware—require stricter controls due to their role in critical surgical procedures. Classification depends on factors like intended use and potential risk to patients.

What kinds of orthopaedic procedures are Flower Orthopedics Corporation’s devices intended for?

Flower Orthopedics Corporation’s devices are designed for orthopaedic procedures including fracture stabilization, joint reconstruction, and bone alignment. Examples include fixation of long bones, joint-specific plates (like MTP plates for the foot), and screws tailored for specific anatomical needs, such as variable-angle compression or headless compression screws for precise internal fixation.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: —
Website: flowerortho.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 8777788587
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 078790947

Catalogue (2233)

Page 3 of 45

Device	Model / Reference	Registries	Class	Status
Cannulated Screw, Partially Threaded	CSP 640	FDA UDI	Class II	Active
Variable Angle Non-Locking Screw	FLS 360	FDA UDI	Class II	Active
1.7mm Two Hole Compression Plate, 2.7mm/3.0mm	FFP 072	FDA UDI	Class II	Active
Flower Orthopedics	PERND	FDA UDI	Class I	Active
Anterior Lateral Distal Tibial Plate Trials	FIS 651	FDA UDI	Class I	Active
Cannulated Screw, Partially Threaded	CSP 620	FDA UDI	Class II	Active
1.5mm Recon T-Plate, 7 Holes, 1.5mm/2.0mm/2.4mm	FHF 727	FDA UDI	Class II	Active
Flower Orthopedics	CSO 107	FDA UDI	Class II	Active
Flower Orthopedics	FTP 001	FDA UDI	Class I	Active
Lag Screw, Fully Threaded	LSF 520	FDA UDI	Class II	Active
Flex-Thread Ulna	FTU 421-S	FDA UDI	Class II	Active
Cannulated Screw, Partially Threaded	CSP 224	FDA UDI	Class II	Active
Lag Screw, Fully Threaded	LSF 570	FDA UDI	Class II	Active
Flex-Thread Ulna	FRS 155	FDA UDI	Class I	Active
Flower Orthopedics	FPSL2756	FDA UDI	Class II	Active
Flower Orthopedics	XRPT314	FDA UDI	Class I	Active
Variable Angle Non-Locking Screw	FLS 310	FDA UDI	Class II	Active
Flower Orthopedics	FPSL4056	FDA UDI	Class II	Active
Cannulated Screw, Fully Threaded	CSF 780	FDA UDI	Class II	Active
1.7mm NC Plate, (R), 2.7mm/3.0mm	FFP 021	FDA UDI	Class II	Active
Cannulated Screw, Partially Threaded	CSP 945	FDA UDI	Class II	Active
Flower Orthopedics	OC73085	FDA UDI	Class II	Active
MIS Guide, Large	CPF 994	FDA UDI	Class I	Active
Flower Orthopedics	XOPT107	FDA UDI	Class I	Active
Lag Screw, Partially Threaded	LSP 320	FDA UDI	Class II	Active
Variable Angle Compression Screw D:2.0 x L: 11mm	FCS 011	FDA UDI	Class II	Active
Snap Off Screw Full Threaded 3.0mm- Length 14mm	FSS 314	FDA UDI	Class II	Active
Compression Y-Plate, 7 Holes, use with 1.5mm/2.0mm/2.4mm Screws	FFP 307	FDA UDI	Class II	Active
Variable Angle Compression Screw D:2.0 x L: 28mm	FCS 028	FDA UDI	Class II	Active
Flower Orthopedics	FPSL2746	FDA UDI	Class II	Active
Variable Angle Compression Screw D:2.0 x L: 22mm	FCS 022	FDA UDI	Class II	Active
Flower Orthopedics	OC65055	FDA UDI	Class II	Active
Headless Compression Screw, D:2.4mm x L: 28mm	HCS 128	FDA UDI	Class II	Active
Flex-Thread Ulna	FTU 621-S	FDA UDI	Class II	Active
Headless Compression Screw, D:2.4mm x L: 6mm	HCS 106	FDA UDI	Class II	Active
Recon Plate, 6 Holes	FRP 706	FDA UDI	Class II	Active
Variable Angle Locking Screw, Low Profile, D:2.7mm x L:55.0mm	FLP 255	FDA UDI	Class II	Active
Cannulated Screw, Partially Threaded	CSP 235	FDA UDI	Class II	Active
Cannulated Screw, Partially Threaded	CSP 835	FDA UDI	Class II	Active
Flower Orthopedics	FPSC2710	FDA UDI	Class II	Active
FlowerToe Cannulated, D:2.0mm x 13mm	FHT 200	FDA UDI	Class II	Active
Headless Compression Screw, D:2.2mm x L: 10mm	HCS 010	FDA UDI	Class II	Active
Low Profile Locking Plate, 8 Holes	FFP 088	FDA UDI	Class II	Active
Variable Angle Non-Locking Screw	FBS 006	FDA UDI	Class II	Active
Flower Orthopedics	XUPT323	FDA UDI	Class I	Active
Fibula Nail, 5.5mm x 180mm, Titanium, Flex-Thread™	8424-15-S	FDA UDI	Class II	Active
Cortex Screw, 3.5mm x 30mm, T15, Flex-Thread™	8428-30-S	FDA UDI	Class II	Active
Variable Angle Compression Screw D:1.5 x L: 08mm	FCS 108	FDA UDI	Class II	Active
Flower Orthopedics	FPSL4068	FDA UDI	Class II	Active
Jones Screw, Short Threaded, D: 6.5mm x L:50mm	FJS 350	FDA UDI	Class II	Active

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FDA Recalls (16)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Flower Orthopedics Corporation has 16 recall records initiated between February 16, 2015, and August 29, 2023. The records include open, classified, and terminated statuses, with reasons involving mechanical failures such as broken cannulated screwdrivers, non-locking pegs, missing or incompatible components (e.g., drill bits without AO connect, missing countersinks, or mismatched inserter parts), and manufacturing errors like incorrect material use in calcaneus plates. Some recalls cite potential delays in surgical procedures or the need for additional interventions due to device malfunctions.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Aug 29, 2023	Z-0074-2024	—	open, classified	Device is breaking while in use, potential for patients to require a revision surgery.
Nov 2, 2021	Z-0448-2022	—	terminated	Mating incompatibility between the Inserter Shaft and the Inserter Draw Rod causing the inserter draw rod to bind and not rotate freely as intended surgeon may be unable to complete surgery unless a second set is available
Sep 3, 2021	Z-0034-2022	—	terminated	Product kit missing CDG 200 (Cannulated Countersink for 3.0-4.5mm Screws) from EWK 201 (Flower E-Kit, Advanced)
Sep 1, 2021	Z-0113-2022	—	terminated	Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Sep 1, 2021	Z-0114-2022	—	terminated	Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Sep 1, 2021	Z-0112-2022	—	terminated	Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Sep 1, 2021	Z-0111-2022	—	terminated	Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Apr 15, 2021	Z-1698-2021	—	terminated	Cannulated Screwdrivers may break at the driver tip along the shaft, near the handle extending surgery time and additional x-ray to identify the fragments from the breakages
Jul 8, 2020	Z-2785-2020	—	terminated	The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
Jul 8, 2020	Z-2783-2020	—	terminated	The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
Jul 8, 2020	Z-2784-2020	—	terminated	The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
Jul 8, 2020	Z-2786-2020	—	terminated	The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
Jul 8, 2020	Z-2787-2020	—	terminated	The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
Jul 8, 2020	Z-2782-2020	—	terminated	The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
Dec 22, 2016	Z-1113-2017	—	terminated	The product is being recalled due to incidence and reports of the product breaking during surgery.
Feb 16, 2015	Z-1314-2015	—	terminated	Locking pegs were not locking during distal radius procedures. There has been one (1) report of revision surgery scheduled to remove a loosened peg.