Bur, surgical, general & plastic surgery: medical device reports filed with FDA

2,113 reports carry this product code, 1993–2026; 15 brands with a page.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

2,113
reports with this product code: 0% of all MAUDE reports; 95
reports, 12 months to August 2026: 80 in the 12 months before; 90.6%
classified as malfunction: 62.3% across all reports; 0%
classified as death, as reported: 0.9% across all reports

Product code GFF is FDA's classification for "Bur, surgical, general & plastic surgery" (general, Plastic Surgery panel), a class 1 device. 2,113 medical device reports carry this product code, 0% of the MAUDE database, from September 1993 to August 2026.

95 reports arrived in the 12 months to August 2026, up 19% from 80 in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (90.6%), injury (8.2%) and other (0.5%). 15 brand names with a page on this site carry this code; the brands table is ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Brands with this product code

Brand	Reports	Latest 12 months	Classified as death	Classified as malfunction
Standard Craniotome Black Max	157	0	0%	98.7%
1 85mm X 16mm Fluted Router	36	0	0%	94.8%
4 0mm Aggressive Plus Cutter Formula 5bx	36	0	0%	94.7%
Unknown_InstrumentstIre_Product	13	123	0%	97.4%
2 15mm X 22mm Spiral Router	10	0	0%	100%
2 5mm Drill Bit/Qc/Gold/110mm	6	14	0%	74.1%
Cable Tensioner	6	0	0%	96.4%
Sterling	6	300	0.1%	95.6%
8cm Angle Attachment	5	6	0%	99.7%
Conmed	5	89	0.2%	65.6%
2 0mm Cannulated Drill Bit/Qc 150mm	1	3	0%	70.5%
Microaire	1	0	0.6%	67.6%
Stryker	1	5	1.3%	46.3%
Synthes	1	0	0.6%	36.4%
Twist Drill	1	0	0%	10.6%

Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Manufacturers named

Manufacturer (as written on reports)	Reports	Share
Depuy Synthes Power Tools	941	44.5%
Stryker Endoscopy-San Jose	129	6.1%
Conmed	91	4.3%
The Anspach Effort	57	2.7%
Arthrex	39	1.8%
Stryker Ireland	28	1.3%
Depuy Synthes Products	26	1.2%
Conmed Linvatec	15	0.7%
Stryker Endoscopy Puerto Rico	8	0.4%
Stryker Endoscopy	7	0.3%
Biomet 3i	2	0.1%
Stryker Instruments	2	0.1%
Dentsply Maillefer	1	0%
Linvatec	1	0%
Richard Wolf	1	0%

Reports by month, five years

FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.

Event type and report source

Event type

Death0%0

Injury8.2%173

Malfunction90.6%1,915

Other0.5%10

Not given0.7%15

Who filed

Manufacturer report96.9%2,048

Voluntary report1.5%32

User facility report0%0

Distributor report0.1%3

Not given1.4%30

Grey bar: all 26,136,888 MAUDE reports.

Device problems coded

Device problem (FDA code)	Reports	Share
Breakthe device broke	694	32.8%
Device contamination with chemical or other material	205	9.7%
Device operates differently than expectedthe device behaved unexpectedly	159	7.5%
Material fragmentation	148	7%
Packaging problem	130	6.2%
Overheating of device	125	5.9%
Fracturea broken bone	79	3.7%
Bent	78	3.7%
Detachment of device component	71	3.4%
Metal shedding debris	46	2.2%
Device packaging compromised	45	2.1%
Device inoperablethe device could not be used	40	1.9%
Temperature problem	39	1.8%
Material twisted/bent	34	1.6%
Detachment of device or device componentpart of the device came off	33	1.6%
Difficult to insertthe device was hard to insert	30	1.4%
Failure to cut	28	1.3%
Sticking	22	1%
Defective devicethe device was defective	20	0.9%
Component falling	18	0.9%

Questions about bur, surgical, general & plastic surgery reports

What is product code GFF?

FDA's classification code for "Bur, surgical, general & plastic surgery", class 1, reviewed by the general, Plastic Surgery panel. Every device report carries the product code of the device involved.

How many reports carry this code?

2,113 reports through August 2026, 95 of them in the latest 12 months.

Which brands appear most often?

Standard Craniotome Black Max (157), 1 85mm X 16mm Fluted Router (36), 4 0mm Aggressive Plus Cutter Formula 5bx (36), Unknown_InstrumentstIre_Product (13) and 2 15mm X 22mm Spiral Router (10). Widely used products collect more reports because more people use them.

Can the brands table be used to rank the devices?

No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." Brands differ in how many are in use, how long they have been sold and how reports are collected.

Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.

Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.