Flower Orthopedics Corporation
Flower Orthopedics Corporation holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2020, with 16 FDA device recalls on record.
Top product codes for Flower Orthopedics Corporation
FDA recalls by Flower Orthopedics Corporation
10 most recent of 16- Z-0074-2024 — Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to ream and subsequently open the intramedullary canal to the appropriate depth for nail insertion; Flex-Thread TM 3.2mm is provided sterile, single use. Catalogue Number: 8528-1-S
- Z-0448-2022 — Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue Ratchet Handle in order to facilitate the insertion of the Flex-Thread Nail System- Catalog Number: 8435-1
- Z-0034-2022 — Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201
- Z-0111-2022 — Flower Drill Bit Kit 2.0 mm - intended to be used with solid 2.0mm screws and can be used with any plate that has been cleared as part of the Flower Small and Medium Implant Set and uses the small locking mechanism. mechanism. Catalog Number: DBK 020 2013002721
- Z-0114-2022 — Flower Lag Screw Kit 2.7 mm-intended to be used with 2.7mm lag screws and can be used with any plate that as part of the Flower Small and Medium Implant Set, Flower Ankle Plating Set , Flower Rear Foot/Calcaneus Plating Set , or Flower Upper Extremity Plating Set and uses the medium locking mechanism. Catalog Number: LSK 027
- Z-0112-2022 — Flower Drill Bit Kit 2.4 mm-intended to be used with solid 2.4mm screws and can be used with any plate as part of the Flower Small and Medium Implant Set and uses the small locking mechanism. Catalog Number: DBK 024
- Z-0113-2022 — Flower Drill Bit Kit 2.7mm- The Drill Bit Kit, 2.7mm (DBK 027) is intended to be used with solid 2.7mm screws and can be used with any the Flower Small and Medium Implant Set Flower Ankle Plating Set , Flower Rear Foot/Calcaneus Plating Set or Flower Upper Extremity Plating Set and uses the medium locking mechanism. Catalog Number: DBK 027
- Z-1698-2021 — T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits (GWK 300) - Product Usage: Intended to be used to insert screws with T25 driving features, which includes screws with diameters of 5.5mm, 6.5mm, and 7.3mm Product Code: GWK 300
- Z-2785-2020 — Calcaneus Plate, Extensile, Small, Right, Catalog Number CPF 201 - Product Usage: intended to be used for internal fixation of fractures and reconstruction of bones of the rearfoot, including the calcaneus.
- Z-2782-2020 — Calcaneus Plate, Extensile, Small, Left, Catalog Number CPF 101 - Product Usage: intended to be used for internal fixation of fractures and reconstruction of bones of the rearfoot, including the calcaneus.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Flower Orthopedics Corporation
- K192949 — Flower Suture Anchor Set
- K170687 — Flower Bone Screw Set
- K142306 — Flower Upper Extremity Plating Set
- K133930 — FLOWER REAR FOOT PLATING SET, FLOWER CALCANEUS PLANTING SET, FLOWER REARFOOT PLATING SET
- K133102 — FLOWER ANKLE PLATING SET
- K132248 — FLOWER BONE SCREW SET
- K131657 — FLOWER SMALL AND MEDIUM IMPLANT SET
- K123562 — FLOWER SMALL AND MEDIUM BONE IMPLANTS
Data sourced from openFDA. This site is unofficial and independent of the FDA.