510(k) · Cleared
Clearedrestor3d Pin Implants
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Restor3D · HTY Pin, Fixation, Smooth
Cleared on Jan 4, 2022 as substantially equivalent to K181180 (OSSIO, Ltd., 2019) after a 208-day review. Its family tree reaches back 4 generations to 1990.
- Decided
- Jan 4, 2022
- Review
- 208 days
- Class
- Class II
- Product code
- HTY
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K901456 (1990). 6 ancestors in all. No later device cites it as a predicate yet.
- Root · 4 generations backK901456 Orthosorb (R) Absorbable PinJohnson & Johnson International · 1990
- 3 generations backK031712 Inion Otps Biodegradable PinInion, Ltd. · 2003
- 2 generations backK050275 Modification to: Inion Otps Biodegradable PinInion, Ltd. · 2005
- 1 generation backK181180 OSSIO™ Pin Product FamilyOSSIO, Ltd. · 2019
- This deviceK211789 restor3d Pin ImplantsRestor3D · 2022
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K901456 | Orthosorb (R) Absorbable Pin | Johnson & Johnson International | 1990 | — |
| −3 | K031712 | Inion Otps Biodegradable Pin | Inion, Ltd. | 2003 | — |
| −2 | K050275 | Modification to: Inion Otps Biodegradable Pin | Inion, Ltd. | 2005 | — |
| −1 | K181180 | OSSIO™ Pin Product Family | OSSIO, Ltd. | 2019 | — |
| 0 (this device) | K211789 | restor3d Pin Implants | Restor3D | 2022 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
| 2001 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in HTY? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new HTY device
- #1 K231272 OSSIOfiber® Pin Product Family, OSSIOfiber®…score 19.3 · 14 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K181180 | OSSIO™ Pin Product FamilySummary page 4…tener Regulation Class: Class II Product Code: HTY E. Predicate Devices: Primary Predicate: OSSIOTM Pin Product Family (K181180) Reference Predicates: Arthrex Bio-Pin (K050259) ADI TiDAL Osteotomy Wedge (K… | 2019 |
| † | K050259 | Arthrex Bio-Pin | 2005 |
| † | K191047 | ADI TiDAL Osteotomy Wedge | 2019 |
| † | K143618 | Kirschner Wires, Steinmann Pins | 2015 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 32 years and passes through 4 companies; a new generation was cleared every 13.0 years on median.
- None of the 6 ancestors has a recall.
- 4 other devices also cite its predicate K181180.
How does its category compare?
All HTY devicesHTY Pin, Fixation, Smooth: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.
FDA decisions per year · HTY
5in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HTY
90in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HTY
2in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HTY
39in 2025
MAUDE reports naming product code HTY, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 6 | 112 | 0 | 46 |
| 2008 | 6 | 86 | 0 | 38 |
| 2009 | 2 | — | 1 | 36 |
| 2010 | 9 | 180 | 1 | 33 |
| 2011 | 6 | 82 | 0 | 164 |
| 2012 | 4 | 76 | 0 | 129 |
| 2013 | 4 | 128 | 0 | 187 |
| 2014 | 8 | 73 | 0 | 149 |
| 2015 | 8 | 101 | 0 | 121 |
| 2016 | 6 | 114 | 2 | 128 |
| 2017 | 5 | 127 | 0 | 82 |
| 2018 | 4 | 162 | 0 | 138 |
| 2019 | 4 | 93 | 1 | 222 |
| 2020 | 5 | 108 | 0 | 210 |
| 2021 | 5 | 137 | 0 | 148 |
| 2022 | 4 | 121 | 2 | 96 |
| 2023 | 5 | 146 | 0 | 153 |
| 2024 | 1 | — | 0 | 297 |
| 2025 | 5 | 90 | 0 | 39 |
| 2026 | 2 | — | 1 | — |
What is it indicated for?
restor3d Pin Implants are indicated for maintenance of alignment and fixation of bone fractures, osteotomies, arthrodesis, and bone grafts in the presence of appropriate additional immobilization (e.g. rigid fixation implants, cast, brace).
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K211789 · printed Nov 6, 2026
Cite this page
510(k) Report. “K211789: restor3d Pin Implants.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K211789
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026