EJE: Frame, Rubber Dam
FDA product code EJE. Class I, classified under 21 CFR 872.6300. What the classification flags say about Part 820 under the QMSR.
Classification
- Product code
- EJE
- Device name
- Frame, Rubber Dam
- Device class
- Class I
- Regulation
- 21 CFR 872.6300
- Review panel
- Dental
- Premarket route
- 510(k) exempt
- CGMP-exempt flag
- Yes
- Life-sustaining flag
- No
- Implant flag
- No
- Third-party review
- Not a candidate
- Summary malfunction reporting
- Eligible
Data from openFDA as of 26 October 2026. Read the record on openFDA · FDA product code classification database
Part 820 requirements the flags point to
Part 820 rules for EJE
- CGMP exemptionClassification regulation, 21 CFR parts 862 to 892
- Exemption flaggedFDA flags this product code as exempt from CGMP.The exemption is in the classification regulation, 21 CFR 872.6300, as it stood on 2026-11-05. In this text the exemption depends on the device not being labeled or represented as sterile, which the flag does not record. FDA states that exemption from CGMP does not exempt a finished-device manufacturer from keeping complaint files or from the records 21 CFR 820.35 requires.
The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 872.9. If the device is not labeled or otherwise represented as sterile, it is exempt from the current good manufacturing practice requirements of the quality management system regulation in part 820 of this chapter, except for requirements concerning records and complaint files under § 820.35 of this chapter.21 CFR 872.6300
FDA: QMSR, CGMP exemptions · 21 CFR 820.35 - Design and development, ISO 13485 clause 7.321 CFR 820.10(c)
- Database cannot sayClass I: clause 7.3 applies only if the device is automated with computer software.This code's regulation (872.6300) is not on the 820.10(c)(2) table. The other route in is 820.10(c)(1), class I devices automated with computer software. The database has no software field, so it cannot answer that. The CGMP exemption flag also applies to this code.21 CFR 820.10
- Traceability, ISO 13485 clause 7.5.9.221 CFR 820.10(d)
- Not flaggedFDA does not flag this code as life-supporting or life-sustaining.820.10(d) is not indicated by this flag.21 CFR 820.10 · 21 CFR 860.3 · QMSR final rule, comment 49
- Complaint and record content21 CFR 820.35
- Rule names this classApplies to every finished-device manufacturer, exempt or not.820.35 adds content to complaint records, servicing records and UDI recording on top of ISO 13485 clause 4.2.5. FDA says CGMP exemption does not lift these records.21 CFR 820.35 · FDA: QMSR, CGMP exemptions
These flags describe the classification of a product code. They are not a determination for a specific device or manufacturer. How a manufacturer meets 21 CFR 820.10 depends on its own device, its intended use and the full text of the rule.
Clearances and recalls on record
- 510(k), De Novo and BK numbers linked
- 3 · Search these clearances
- PMA numbers linked
- 0
- Recall product records
- 0
- Adverse event reports
- Search MAUDE for EJE
Recall records count products, and one recall event can add many. Counts show activity in a category. They do not measure its safety.
Search all 7,097 product codes, or read the guide to the Part 820 rules behind these flags.
Check your quality documents against Part 820
Arca puts your SOPs and design files in a library and compares them against the Part 820 requirements for your device in a grid, one row per document and one column per requirement, with each cell cited to its source.