510(k) Report

FDA product code · Radiology

Hydrogel Spacer

OVBClass II21 CFR 892.5725510(k) required8 decisions since 20152 recalls

8 FDA decisions since 2015. 510(k) reviews decided 2021–2025 took a median of 208 days (half between 145 and 270). 2 recalls name this code, 0 of them Class I. The most-cited predicate is DEN140030, named by 3 later devices.

The perirectal spacer is intended to temporarily position the anterior rectal wall away from the prostate during radiotherapy for prostate cancer and in creating this space it is the intent of the perirectal spacer to reduce the radiation dose delivered to the anterior rectum. The perirectal spacer is composed of biodegradable material and maintains space for the entire course of prostate radiotherapy treatment and…

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, radiology panel

Twenty years of OVB at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · OVB

2so far in 2026, the most since 2007

2015: 12018: 12019: 12020: 12022: 12023: 12026 (partial year): 2
2007high 2 (2026) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OVB

Too few OVB 510(k)s in any year since 2007 to give a median.

Recalls per year · OVB

2in 2022

2022: 2
2007high 2 (2022) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · OVB

339in 2025

2016: 22017: 32018: 112019: 852020: 1262021: 2722022: 3872023: 3272024: 3292025: 339
2007high 387 (2022) · low 0 (2007)2025

MAUDE reports naming product code OVB, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20151—00
20160—02
20170—03
20181—011
20191—085
20201—0126
20210—0272
20221—2387
20231—0327
20240—0329
20250—0339
20262—0—
FIG. 1 — OVB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OVB? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report