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UNI-CLIP

NEWDEAL · Model 213216ND · UDI-DI 10381780052609

JDR Prescription
10
510(k) clearances
2,692
Adverse events
37
Recalls
242
Facilities

Description

The UNI-CLIP STAPLE is designed so that, by widening the diamond shaped opening, mechanical deformation leads to narrowing of the interaxis of the two legs. The surgeon can obtain a true compression, adjustable and controlled with many choice of sizes (11, 12, 13 or 15mm interaxis, and lengths vary from 13 to 20mm). The UNI-CLIP STAPLE is made from Stainless Steel and it is indicated for fixation of bone fractures or for bone reconstruction. It is delivered non sterile.

Recalls

DateFirmReason
2026-07-15F & A FoundationBone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established.
2026-05-11In2bones USA, LLCDue to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.
2022-09-27Synthes (USA) Products LLCThe subject products are being recalled because they contain the incorrect size drill guide and will not prepare the bone correctly for the size of the implant included in the ster
2022-09-27Synthes (USA) Products LLCThe subject products are being recalled because they contain the incorrect size drill guide and will not prepare the bone correctly for the size of the implant included in the ster
2022-09-27Synthes (USA) Products LLCThe subject products are being recalled because they contain the incorrect size drill guide and will not prepare the bone correctly for the size of the implant included in the ster
2022-09-27Synthes (USA) Products LLCThe subject products are being recalled because they contain the incorrect size drill guide and will not prepare the bone correctly for the size of the implant included in the ster
2022-08-30Synthes (USA) Products LLCDrill Pin (drill bit) is not compatible with the Drill Template included in the kit due to a packaging error, result in a surgical delay and may cause soft tissue damage if a larg
2022-03-10Wright Medical Technology, Inc.The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.
2022-02-14Biomet, Inc.Packaging of various implants may not have sufficient adhesion on all sides, leading to loss of sterile barrier integrity. Use of product poses risk of infection, leading to surgic
2022-02-14Biomet, Inc.Packaging of various implants may not have sufficient adhesion on all sides, leading to loss of sterile barrier integrity. Use of product poses risk of infection, leading to surgic

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.